geneid | 25821 |
---|---|
ensemblid | ENSG00000135297.17 |
hgncid | 19261 |
symbol | MTO1 |
name | mitochondrial tRNA translation optimization 1 |
refseq_nuc | NM_012123.4 |
refseq_prot | NP_036255.2 |
ensembl_nuc | ENST00000498286.6 |
ensembl_prot | ENSP00000419561.2 |
mane_status | MANE Select |
chr | chr6 |
start | 73461737 |
end | 73509236 |
strand | + |
ver | v1.2 |
region | chr6:73461737-73509236 |
region5000 | chr6:73456737-73514236 |
regionname0 | MTO1_chr6_73461737_73509236 |
regionname5000 | MTO1_chr6_73456737_73514236 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 692 | 391 | 87 | 72 | 183 | 18 | 29 | 141 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0002 | 0/0 | 692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0003 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0004 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0005 | 0/0 | 692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0006 | 0/0 | 692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2079 | 308 | 66 | 59 | 142 | 15 | 25 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0002 | 0/0 | 2079 | 80 | 19 | 13 | 41 | 3 | 4 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0003 | 0/0 | 2079 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0004 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0005 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0006 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0007 | 0/1 | 2079 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0008 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
c0009 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 9300 | 50 | 16 | 6 | 20 | 3 | 5 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0002 | 0/0 | 9318 | 29 | 0 | 4 | 21 | 2 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0003 | 0/0 | 9312 | 24 | 0 | 8 | 14 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0004 | 0/0 | 9307 | 22 | 0 | 6 | 16 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0005 | 0/0 | 8620 | 17 | 0 | 3 | 12 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0006 | 0/1 | 9300 | 17 | 1 | 5 | 3 | 2 | 5 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0007 | 0/0 | 9301 | 16 | 3 | 0 | 11 | 1 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0008 | 0/0 | 8619 | 10 | 7 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0009 | 0/0 | 9301 | 9 | 6 | 1 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0010 | 0/0 | 9314 | 8 | 6 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0011 | 0/0 | 9319 | 8 | 0 | 3 | 3 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0012 | 0/0 | 9300 | 7 | 0 | 3 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0013 | 0/0 | 9300 | 7 | 0 | 5 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0014 | 0/0 | 9315 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0015 | 0/0 | 9314 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0016 | 0/0 | 9313 | 6 | 1 | 0 | 5 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0017 | 0/0 | 8620 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0018 | 0/0 | 9300 | 4 | 0 | 0 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0019 | 0/0 | 9312 | 4 | 0 | 1 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0020 | 0/0 | 9310 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0021 | 0/0 | 9306 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0022 | 1/0 | 8620 | 3 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0023 | 0/0 | 9303 | 3 | 0 | 1 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0024 | 0/0 | 9301 | 3 | 0 | 0 | 0 | 0 | 3 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0025 | 0/0 | 9314 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0026 | 0/0 | 9317 | 3 | 0 | 1 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0027 | 0/0 | 9317 | 3 | 2 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0028 | 0/0 | 9309 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0029 | 0/0 | 9307 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0030 | 0/0 | 9301 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0031 | 0/0 | 8620 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0032 | 0/0 | 9308 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0033 | 0/0 | 9313 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0034 | 0/0 | 9300 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0035 | 0/0 | 9303 | 2 | 1 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0036 | 0/0 | 9300 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0037 | 0/0 | 9313 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0038 | 0/0 | 9317 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0039 | 0/0 | 9319 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0040 | 0/0 | 9300 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0041 | 0/0 | 8621 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0042 | 0/0 | 8619 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0043 | 0/0 | 8621 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0044 | 0/0 | 8622 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0045 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0046 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0047 | 0/0 | 8617 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0048 | 0/0 | 8620 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0049 | 0/0 | 8620 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0050 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0051 | 0/0 | 9307 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0052 | 0/0 | 9314 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0053 | 0/0 | 9314 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0054 | 0/0 | 9320 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0055 | 0/0 | 9307 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0056 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0057 | 0/0 | 9315 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0058 | 0/0 | 9315 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0059 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0060 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0061 | 0/0 | 9306 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0062 | 0/0 | 9314 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0063 | 0/0 | 9319 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0064 | 0/0 | 9318 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0065 | 0/0 | 9301 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0066 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0067 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0068 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0069 | 0/0 | 9300 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0070 | 0/0 | 9301 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0071 | 0/0 | 9317 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0072 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0073 | 0/0 | 9302 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0074 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0075 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0076 | 0/0 | 9302 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0077 | 0/0 | 9301 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0078 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0079 | 0/0 | 9300 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0080 | 0/0 | 9300 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0081 | 0/0 | 9299 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0082 | 0/0 | 9300 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0083 | 0/0 | 9302 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0084 | 0/0 | 9301 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0085 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0086 | 0/0 | 9302 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0087 | 0/0 | 9301 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0088 | 0/0 | 9302 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0089 | 0/0 | 9301 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0090 | 0/0 | 9303 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0091 | 0/0 | 9302 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0092 | 0/0 | 9313 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0093 | 0/0 | 9300 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0094 | 0/0 | 9300 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0095 | 0/0 | 9317 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0096 | 0/0 | 9314 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0097 | 0/0 | 9313 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0098 | 0/0 | 9313 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0099 | 0/0 | 9313 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0100 | 0/0 | 9313 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0101 | 0/0 | 9314 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0102 | 0/0 | 9305 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0103 | 0/0 | 9312 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0104 | 0/0 | 9315 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0105 | 0/0 | 9313 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0106 | 0/0 | 9312 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0107 | 0/0 | 9313 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0108 | 0/0 | 9313 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0109 | 0/0 | 9312 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0110 | 0/0 | 9318 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0111 | 0/0 | 9318 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0112 | 0/0 | 9319 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0113 | 0/0 | 9316 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0114 | 0/0 | 9318 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0115 | 0/0 | 9316 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0116 | 0/0 | 9319 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0117 | 0/0 | 9320 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0118 | 0/0 | 9319 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0119 | 0/0 | 9318 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0120 | 0/0 | 9317 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0121 | 0/0 | 9312 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0122 | 0/0 | 9312 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0123 | 0/0 | 9310 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0124 | 0/0 | 9307 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0125 | 0/0 | 9306 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0126 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0127 | 0/0 | 9306 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
t0128 | 0/0 | 9301 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0005 | 0/1 | 3 | 0 | 0 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2079 | 308 | 66 | 59 | 142 | 15 | 25 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002 | 0/0 | 2079 | 80 | 19 | 13 | 41 | 3 | 4 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0003 | 0/0 | 2079 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0007 | 0/1 | 2079 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0002c0009 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0003c0004 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0004c0005 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0005c0006 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0006c0008 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11378 | 49 | 16 | 6 | 20 | 3 | 4 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0003 | 0/0 | 11390 | 24 | 0 | 8 | 14 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0004 | 0/0 | 11385 | 21 | 0 | 6 | 15 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0005 | 0/0 | 10698 | 17 | 0 | 3 | 12 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0006 | 0/0 | 11378 | 16 | 1 | 5 | 3 | 2 | 5 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0007 | 0/0 | 11379 | 15 | 3 | 0 | 10 | 1 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0008 | 0/0 | 10697 | 10 | 7 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0009 | 0/0 | 11379 | 9 | 6 | 1 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0010 | 0/0 | 11392 | 7 | 5 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0012 | 0/0 | 11378 | 7 | 0 | 3 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0013 | 0/0 | 11378 | 7 | 0 | 5 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0014 | 0/0 | 11393 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0015 | 0/0 | 11392 | 6 | 0 | 0 | 6 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0016 | 0/0 | 11391 | 6 | 1 | 0 | 5 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0017 | 0/0 | 10698 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0018 | 0/0 | 11378 | 4 | 0 | 0 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0019 | 0/0 | 11390 | 4 | 0 | 1 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0022 | 1/0 | 10698 | 3 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0023 | 0/0 | 11381 | 3 | 0 | 1 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0024 | 0/0 | 11379 | 3 | 0 | 0 | 0 | 0 | 3 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0025 | 0/0 | 11392 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0031 | 0/0 | 10698 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0032 | 0/0 | 11386 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0033 | 0/0 | 11391 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0034 | 0/0 | 11378 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0035 | 0/0 | 11381 | 2 | 1 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0036 | 0/0 | 11378 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0037 | 0/0 | 11391 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0040 | 0/0 | 11378 | 2 | 0 | 1 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0041 | 0/0 | 10699 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0042 | 0/0 | 10697 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0043 | 0/0 | 10699 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0044 | 0/0 | 10700 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0045 | 0/0 | 10697 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0046 | 0/0 | 10697 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0047 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0048 | 0/0 | 10698 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0049 | 0/0 | 10698 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0050 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0051 | 0/0 | 11385 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0052 | 0/0 | 11392 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0053 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0054 | 0/0 | 11398 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0055 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0056 | 0/0 | 11387 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0057 | 0/0 | 11393 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0058 | 0/0 | 11393 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0059 | 0/0 | 11386 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0060 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0061 | 0/0 | 11384 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0062 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0065 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0066 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0067 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0068 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0069 | 0/0 | 11378 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0070 | 0/0 | 11379 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0071 | 0/0 | 11395 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0072 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0073 | 0/0 | 11380 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0074 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0075 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0076 | 0/0 | 11380 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0077 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0078 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0079 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0080 | 0/0 | 11378 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0081 | 0/0 | 11377 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0082 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0083 | 0/0 | 11380 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0084 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0085 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0086 | 0/0 | 11380 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0087 | 0/0 | 11379 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0088 | 0/0 | 11380 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0089 | 0/0 | 11379 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0090 | 0/0 | 11381 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0091 | 0/0 | 11380 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0092 | 0/0 | 11391 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0093 | 0/0 | 11378 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0094 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0095 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0096 | 0/0 | 11392 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0097 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0098 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0099 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0100 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0101 | 0/0 | 11392 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0102 | 0/0 | 11383 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0103 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0104 | 0/0 | 11393 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0105 | 0/0 | 11391 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0106 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0107 | 0/0 | 11391 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0108 | 0/0 | 11391 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0109 | 0/0 | 11390 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0001t0128 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0002 | 0/0 | 11396 | 29 | 0 | 4 | 21 | 2 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0011 | 0/0 | 11397 | 8 | 0 | 3 | 3 | 0 | 2 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0020 | 0/0 | 11388 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0021 | 0/0 | 11384 | 4 | 4 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0026 | 0/0 | 11395 | 2 | 0 | 1 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0027 | 0/0 | 11395 | 3 | 2 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0028 | 0/0 | 11387 | 3 | 3 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0029 | 0/0 | 11385 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0038 | 0/0 | 11395 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0039 | 0/0 | 11397 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0063 | 0/0 | 11397 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0064 | 0/0 | 11396 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0110 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0111 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0112 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0113 | 0/0 | 11394 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0114 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0115 | 0/0 | 11394 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0116 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0117 | 0/0 | 11398 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0118 | 0/0 | 11397 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0119 | 0/0 | 11396 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0120 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0121 | 0/0 | 11390 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0122 | 0/0 | 11390 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0123 | 0/0 | 11388 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0124 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0125 | 0/0 | 11384 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0126 | 0/0 | 11386 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0002t0127 | 0/0 | 11384 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0003t0030 | 0/0 | 11379 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0001c0007t0006 | 0/1 | 11378 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0002c0009t0010 | 0/0 | 11392 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0003c0004t0007 | 0/0 | 11379 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0004c0005t0026 | 0/0 | 11395 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0005c0006t0004 | 0/0 | 11385 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
a0006c0008t0001 | 0/0 | 11378 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | copy fasta | chr6 | 73456737 | 73514236 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0014g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0015g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0016g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0017g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0019g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0022g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0023g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0023g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0024g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0025g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0031g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0031g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0032g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0032g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0033g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0034g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0034g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0035g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0035g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0036g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0036g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0037g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0037g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0040g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0040g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0041g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0042g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0043g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0044g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0045g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0046g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0047g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0048g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0049g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0050g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0051g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0052g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0053g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0054g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0055g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0056g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0057g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0058g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0059g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0060g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0061g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0062g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0065g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0066g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0067g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0068g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0069g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0070g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0071g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0072g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0073g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0074g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0075g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0076g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0077g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0078g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0079g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0080g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0081g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0082g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0083g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0084g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0085g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0086g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0087g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0088g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0089g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0090g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0091g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0092g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0093g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0094g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0095g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0096g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0097g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0098g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0099g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0100g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0101g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0102g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0103g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0104g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0105g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0106g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0107g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0108g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0109g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0001t0128g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0026g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0026g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0028g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0029g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0038g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0038g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0039g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0039g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0063g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0064g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0110g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0111g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0112g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0113g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0114g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0115g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0116g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0117g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0118g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0119g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0120g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0121g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0122g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0123g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0124g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0125g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0126g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0002t0127g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0003t0030g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0003t0030g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0001c0007t0006g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0002c0009t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0003c0004t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0004c0005t0026g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0005c0006t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
a0006c0008t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00099 | hp2 | a0001 | c0001 | t0023 | g0005 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00140 | hp1 | a0001 | c0001 | t0094 | g0166 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00140 | hp2 | a0001 | c0001 | t0040 | g0193 | EUR | GBR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00280 | hp1 | a0001 | c0001 | t0034 | g0149 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0148 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00323 | hp2 | a0001 | c0001 | t0082 | g0259 | EUR | FIN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00408 | hp1 | a0001 | c0001 | t0068 | g0226 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00408 | hp2 | a0001 | c0001 | t0037 | g0013 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00438 | hp1 | a0001 | c0001 | t0080 | g0175 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00438 | hp2 | a0001 | c0002 | t0039 | g0023 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00558 | hp2 | a0001 | c0001 | t0012 | g0167 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00597 | hp1 | a0001 | c0001 | t0018 | g0160 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0180 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00642 | hp2 | a0001 | c0001 | t0023 | g0190 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0255 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0258 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00733 | hp2 | a0001 | c0002 | t0026 | g0006 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00735 | hp2 | a0001 | c0001 | t0109 | g0011 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0335 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG00741 | hp2 | a0001 | c0001 | t0091 | g0125 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01070 | hp1 | a0001 | c0002 | t0038 | g0032 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01070 | hp2 | a0001 | c0001 | t0089 | g0248 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01074 | hp2 | a0001 | c0001 | t0041 | g0350 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0249 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0265 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01109 | hp2 | a0001 | c0002 | t0027 | g0090 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01168 | hp1 | a0001 | c0002 | t0064 | g0318 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01168 | hp2 | a0001 | c0001 | t0071 | g0237 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0266 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01169 | hp2 | a0001 | c0002 | t0063 | g0317 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01175 | hp1 | a0001 | c0001 | t0012 | g0123 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0309 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0176 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0181 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01256 | hp1 | a0001 | c0001 | t0073 | g0161 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01257 | hp1 | a0001 | c0001 | t0031 | g0351 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01258 | hp1 | a0001 | c0001 | t0031 | g0347 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01261 | hp1 | a0001 | c0002 | t0011 | g0022 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0003 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0016 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01358 | hp2 | a0001 | c0001 | t0034 | g0138 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01433 | hp2 | a0001 | c0001 | t0040 | g0260 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0362 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01496 | hp2 | a0001 | c0002 | t0011 | g0054 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0188 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0049 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0184 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01516 | hp2 | a0001 | c0002 | t0119 | g0070 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0252 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0183 | EUR | IBS | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01884 | hp1 | a0001 | c0002 | t0021 | g0071 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01891 | hp1 | a0001 | c0001 | t0070 | g0129 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0206 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0277 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01928 | hp2 | a0001 | c0002 | t0011 | g0031 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01934 | hp1 | a0001 | c0001 | t0106 | g0119 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0323 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0348 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01943 | hp2 | a0001 | c0001 | t0104 | g0010 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01975 | hp1 | a0001 | c0001 | t0051 | g0282 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01978 | hp1 | a0001 | c0001 | t0044 | g0356 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01978 | hp2 | a0001 | c0001 | t0012 | g0244 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01993 | hp1 | a0001 | c0001 | t0012 | g0217 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01993 | hp2 | a0001 | c0002 | t0038 | g0030 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02004 | hp1 | a0001 | c0001 | t0052 | g0278 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02004 | hp2 | a0001 | c0001 | t0019 | g0116 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02015 | hp1 | a0001 | c0001 | t0075 | g0231 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02027 | hp1 | a0001 | c0001 | t0128 | g0139 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0122 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02055 | hp1 | a0001 | c0001 | t0048 | g0339 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02055 | hp2 | a0001 | c0001 | t0088 | g0189 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0233 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02074 | hp1 | a0001 | c0001 | t0018 | g0159 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02080 | hp2 | a0001 | c0002 | t0039 | g0040 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0120 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02132 | hp1 | a0001 | c0002 | t0116 | g0063 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02132 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02135 | hp2 | a0001 | c0001 | t0078 | g0156 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02145 | hp2 | a0001 | c0001 | t0093 | g0192 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02155 | hp1 | a0001 | c0002 | t0110 | g0046 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02165 | hp1 | a0001 | c0002 | t0124 | g0008 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02165 | hp2 | a0001 | c0001 | t0012 | g0224 | EAS | CDX | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02257 | hp1 | a0001 | c0002 | t0020 | g0072 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0340 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02273 | hp1 | a0001 | c0001 | t0107 | g0107 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02273 | hp2 | a0001 | c0001 | t0103 | g0009 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02280 | hp2 | a0002 | c0009 | t0010 | g0275 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02300 | hp2 | a0001 | c0001 | t0102 | g0108 | AMR | PEL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02451 | hp1 | a0001 | c0002 | t0113 | g0006 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02451 | hp2 | a0001 | c0001 | t0069 | g0250 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02572 | hp2 | a0001 | c0002 | t0125 | g0086 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02615 | hp1 | a0001 | c0002 | t0122 | g0085 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0304 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02622 | hp2 | a0001 | c0001 | t0025 | g0141 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02630 | hp2 | a0001 | c0001 | t0022 | g0332 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02647 | hp1 | a0001 | c0003 | t0030 | g0354 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02647 | hp2 | a0001 | c0001 | t0047 | g0019 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02717 | hp1 | a0001 | c0002 | t0028 | g0074 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02717 | hp2 | a0001 | c0001 | t0099 | g0137 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02738 | hp2 | a0001 | c0002 | t0011 | g0068 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0298 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02818 | hp1 | a0001 | c0002 | t0027 | g0092 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02818 | hp2 | a0001 | c0002 | t0121 | g0081 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02896 | hp1 | a0001 | c0002 | t0020 | g0076 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02896 | hp2 | a0001 | c0001 | t0035 | g0135 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02897 | hp2 | a0001 | c0001 | t0062 | g0017 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02922 | hp2 | a0001 | c0001 | t0025 | g0140 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0338 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02965 | hp2 | a0001 | c0002 | t0021 | g0080 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0336 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0359 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0346 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03041 | hp2 | a0001 | c0002 | t0021 | g0087 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03098 | hp1 | a0001 | c0001 | t0098 | g0319 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0301 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03130 | hp2 | a0001 | c0002 | t0020 | g0078 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03195 | hp1 | a0001 | c0001 | t0076 | g0270 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0142 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0337 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03239 | hp1 | a0001 | c0002 | t0011 | g0007 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03239 | hp2 | a0001 | c0001 | t0024 | g0257 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03453 | hp1 | a0001 | c0001 | t0022 | g0343 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03453 | hp2 | a0001 | c0001 | t0090 | g0124 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03491 | hp1 | a0001 | c0001 | t0043 | g0345 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0361 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0315 | AFR | ESN | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03540 | hp2 | a0001 | c0002 | t0028 | g0077 | AFR | GWD | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0331 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0358 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0219 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03669 | hp2 | a0001 | c0001 | t0024 | g0263 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03688 | hp1 | a0001 | c0001 | t0024 | g0256 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03688 | hp2 | a0001 | c0001 | t0079 | g0162 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03710 | hp1 | a0006 | c0008 | t0001 | g0223 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03710 | hp2 | a0001 | c0001 | t0087 | g0229 | SAS | PJL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03927 | hp1 | a0001 | c0001 | t0077 | g0169 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03927 | hp2 | a0001 | c0001 | t0054 | g0247 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0261 | SAS | BEB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04115 | hp1 | a0001 | c0001 | t0092 | g0222 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0264 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0194 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0187 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18522 | hp1 | a0001 | c0001 | t0017 | g0357 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0302 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | CHB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18612 | hp2 | a0001 | c0001 | t0014 | g0013 | EAS | CHB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0127 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0360 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18943 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18944 | hp1 | a0001 | c0001 | t0015 | g0205 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18944 | hp2 | a0001 | c0001 | t0018 | g0147 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0220 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18946 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18948 | hp1 | a0001 | c0001 | t0015 | g0313 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18948 | hp2 | a0001 | c0002 | t0026 | g0043 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18951 | hp2 | a0001 | c0002 | t0118 | g0368 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18957 | hp1 | a0001 | c0001 | t0016 | g0366 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18957 | hp2 | a0001 | c0001 | t0037 | g0284 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18962 | hp1 | a0001 | c0001 | t0035 | g0177 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18962 | hp2 | a0001 | c0001 | t0057 | g0294 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18965 | hp1 | a0001 | c0001 | t0016 | g0186 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18965 | hp2 | a0001 | c0001 | t0059 | g0321 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0349 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18969 | hp1 | a0001 | c0001 | t0074 | g0221 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18969 | hp2 | a0001 | c0002 | t0029 | g0008 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18972 | hp2 | a0001 | c0001 | t0016 | g0093 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18973 | hp2 | a0001 | c0001 | t0015 | g0297 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18975 | hp2 | a0001 | c0001 | t0101 | g0095 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18978 | hp1 | a0001 | c0001 | t0085 | g0171 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18978 | hp2 | a0004 | c0005 | t0026 | g0028 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18979 | hp1 | a0001 | c0001 | t0032 | g0296 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18980 | hp2 | a0001 | c0001 | t0055 | g0290 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18981 | hp1 | a0001 | c0002 | t0011 | g0061 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18982 | hp2 | a0001 | c0001 | t0081 | g0253 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18984 | hp2 | a0001 | c0001 | t0067 | g0157 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18987 | hp1 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18987 | hp2 | a0001 | c0002 | t0011 | g0029 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18989 | hp2 | a0001 | c0001 | t0049 | g0341 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18990 | hp2 | a0005 | c0006 | t0004 | g0295 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0364 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18991 | hp2 | a0001 | c0001 | t0014 | g0327 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18995 | hp1 | a0001 | c0001 | t0014 | g0286 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18995 | hp2 | a0001 | c0001 | t0014 | g0293 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18999 | hp1 | a0001 | c0001 | t0032 | g0322 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19000 | hp1 | a0001 | c0002 | t0127 | g0082 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19000 | hp2 | a0001 | c0002 | t0117 | g0067 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19001 | hp2 | a0001 | c0001 | t0058 | g0288 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19002 | hp2 | a0001 | c0001 | t0086 | g0150 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19003 | hp2 | a0001 | c0001 | t0014 | g0285 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19007 | hp2 | a0001 | c0001 | t0015 | g0211 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19009 | hp1 | a0001 | c0001 | t0036 | g0164 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19009 | hp2 | a0001 | c0001 | t0033 | g0097 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19010 | hp2 | a0001 | c0001 | t0019 | g0101 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19011 | hp1 | a0001 | c0002 | t0112 | g0365 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19012 | hp1 | a0001 | c0001 | t0096 | g0202 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19012 | hp2 | a0001 | c0001 | t0036 | g0174 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19030 | hp1 | a0001 | c0002 | t0020 | g0075 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19030 | hp2 | a0001 | c0002 | t0126 | g0088 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19043 | hp1 | a0001 | c0002 | t0021 | g0089 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0312 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19055 | hp2 | a0001 | c0001 | t0015 | g0287 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19056 | hp1 | a0003 | c0004 | t0007 | g0311 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0352 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19058 | hp1 | a0001 | c0001 | t0066 | g0154 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19058 | hp2 | a0001 | c0001 | t0061 | g0300 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19062 | hp1 | a0001 | c0001 | t0015 | g0328 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19063 | hp1 | a0001 | c0001 | t0019 | g0105 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0355 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19064 | hp1 | a0001 | c0002 | t0029 | g0083 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19066 | hp1 | a0001 | c0002 | t0111 | g0062 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19067 | hp1 | a0001 | c0001 | t0019 | g0100 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19067 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19077 | hp1 | a0001 | c0001 | t0095 | g0283 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19081 | hp1 | a0001 | c0001 | t0018 | g0144 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19082 | hp1 | a0001 | c0001 | t0056 | g0320 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19082 | hp2 | a0001 | c0001 | t0007 | g0325 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19083 | hp1 | a0001 | c0001 | t0060 | g0173 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19083 | hp2 | a0001 | c0002 | t0115 | g0024 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19085 | hp2 | a0001 | c0002 | t0029 | g0084 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19086 | hp1 | a0001 | c0002 | t0114 | g0033 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19086 | hp2 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19087 | hp2 | a0001 | c0002 | t0011 | g0059 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19088 | hp1 | a0001 | c0001 | t0072 | g0228 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19090 | hp1 | a0001 | c0001 | t0050 | g0151 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19090 | hp2 | a0001 | c0001 | t0108 | g0096 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19091 | hp1 | a0001 | c0001 | t0016 | g0367 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19240 | hp1 | a0001 | c0002 | t0123 | g0073 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA19240 | hp2 | a0001 | c0001 | t0046 | g0329 | AFR | YRI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20129 | hp1 | a0001 | c0002 | t0028 | g0079 | AFR | ASW | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20752 | hp1 | a0001 | c0001 | t0023 | g0005 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20752 | hp2 | a0001 | c0001 | t0065 | g0152 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | TSI | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20905 | hp1 | a0001 | c0001 | t0083 | g0262 | SAS | GIH | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20905 | hp2 | a0001 | c0001 | t0084 | g0216 | SAS | GIH | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0016 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0198 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0126 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02486 | hp2 | a0001 | c0001 | t0053 | g0209 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03471 | hp1 | a0001 | c0002 | t0027 | g0091 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG03471 | hp2 | a0001 | c0001 | t0100 | g0153 | AFR | MSL | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG06807 | hp1 | a0001 | c0003 | t0030 | g0353 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
HG06807 | hp2 | a0001 | c0001 | t0045 | g0344 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18955 | hp1 | a0001 | c0002 | t0120 | g0065 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA18955 | hp2 | a0001 | c0001 | t0042 | g0363 | EAS | JPT | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20300 | hp1 | a0001 | c0001 | t0105 | g0103 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | USA | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA21309 | hp1 | a0001 | c0001 | t0097 | g0143 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0006 | g0005 | REF | REF | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0022 | g0342 | REF | REF | MTO1_chr6_73456737_73514236 | MTO1 | chr6 | 73456737 | 73514236 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73461903
|
A | G | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.49A>G | p.Lys17Glu | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 167/10698 | 49/2079 | 17/692 | chr6 | 73461903 | ||
chr6:73461925
|
G | C | 1 | a0003 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.71G>C | p.Arg24Pro | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 189/10698 | 71/2079 | 24/692 | chr6 | 73461925 | ||
chr6:73466298
|
A | G | 1 | a0006 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.307A>G | p.Ile103Val | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 2/12 | 425/10698 | 307/2079 | 103/692 | chr6 | 73466298 | ||
chr6:73482620
|
G | C | 1 | a0005 | 1 | NA18990.hp2 | missense_variant&splice_region_variant | MODERATE | c.1637G>C | p.Arg546Thr | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/12 | 1755/10698 | 1637/2079 | 546/692 | chr6 | 73482620 | ||
chr6:73492263
|
T | C | 1 | a0004 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1667T>C | p.Val556Ala | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/12 | 1785/10698 | 1667/2079 | 556/692 | chr6 | 73492263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73480725
|
T | C | 2 | a0001c0002a0004c0005 | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
synonymous_variant | LOW | c.1180T>C | p.Leu394Leu | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/12 | 1298/10698 | 1180/2079 | 394/692 | chr6 | 73480725 | ||
chr6:73482147
|
T | C | 1 | a0001c0003 | 2 | HG02647.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.1368T>C | p.Thr456Thr | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/12 | 1486/10698 | 1368/2079 | 456/692 | chr6 | 73482147 | ||
chr6:73497764
|
A | G | 1 | a0001c0007 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.1785A>G | p.Gln595Gln | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/12 | 1903/10698 | 1785/2079 | 595/692 | chr6 | 73497764 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73461744
|
C | G | 119 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(116): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
5_prime_UTR_variant | MODIFIER | c.-111C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 111 | chr6 | 73461744 | |||||
chr6:73461795
|
G | C | 1 | a0001c0001t0050 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/12 | 60 | chr6 | 73461795 | |||||
chr6:73500864
|
C | G | 1 | a0001c0001t0128 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*129C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 129 | chr6 | 73500864 | |||||
chr6:73500897
|
C | T | 11 | a0001c0002t0020a0001c0002t0021a0001c0002t0028others(8): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 162 | chr6 | 73500897 | |||||
chr6:73501230
|
G | T | 1 | a0001c0001t0049 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 495 | chr6 | 73501230 | |||||
chr6:73501545
|
C | G | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*810C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 810 | chr6 | 73501545 | |||||
chr6:73501997
|
A | T | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1262A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1262 | chr6 | 73501997 | |||||
chr6:73502358
|
C | T | 17 | a0001c0002t0002a0001c0002t0011a0001c0002t0026others(14): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1623C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1623 | chr6 | 73502358 | |||||
chr6:73502451
|
AAAAAG | A | 6 | a0001c0002t0021a0001c0002t0029a0001c0002t0124others(3): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1728delAAGA others(1): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1724 | INFO_REALIGN_3_PRIME | chr6 | 73502451 | ||||
chr6:73502601
|
TAAAG | T | 11 | a0001c0002t0020a0001c0002t0021a0001c0002t0028others(8): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1870_*1873delGAAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1870 | INFO_REALIGN_3_PRIME | chr6 | 73502601 | ||||
chr6:73502620
|
C | T | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1885C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 1885 | chr6 | 73502620 | |||||
chr6:73502895
|
C | CA | 23 | a0001c0001t0033a0001c0001t0041a0001c0001t0060others(20): Show | 62 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2173dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr6 | 73502895 | ||||
chr6:73502895
|
C | CAA | 16 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(13): Show | 53 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2172_*2173dupAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr6 | 73502895 | ||||
chr6:73502956
|
T | C | 1 | a0001c0002t0110 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2221T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2221 | chr6 | 73502956 | |||||
chr6:73502996
|
G | A | 2 | a0001c0001t0034a0001c0001t0065 | 3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2261G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2261 | chr6 | 73502996 | |||||
chr6:73503104
|
G | A | 50 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(47): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2369G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2369 | chr6 | 73503104 | |||||
chr6:73503112
|
C | T | 61 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(58): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*2377C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2377 | chr6 | 73503112 | |||||
chr6:73503172
|
A | G | 1 | a0001c0001t0094 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2437A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2437 | chr6 | 73503172 | |||||
chr6:73503288
|
T | A | 2 | a0001c0001t0066a0001c0001t0067 | 2 | NA18984.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2553T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2553 | chr6 | 73503288 | |||||
chr6:73503314
|
T | C | 1 | a0001c0001t0012 | 7 | HG00558.hp2 HG01175.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2579T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2579 | chr6 | 73503314 | |||||
chr6:73503524
|
T | C | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2789T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2789 | chr6 | 73503524 | |||||
chr6:73503670
|
T | C | 21 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(18): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2935T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 2935 | chr6 | 73503670 | |||||
chr6:73503774
|
G | C | 1 | a0001c0001t0013 | 7 | HG00639.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3039G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3039 | chr6 | 73503774 | |||||
chr6:73503795
|
T | G | 1 | a0001c0001t0068 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3060 | chr6 | 73503795 | |||||
chr6:73503884
|
T | C | 1 | a0001c0002t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3149T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3149 | chr6 | 73503884 | |||||
chr6:73504232
|
A | G | 1 | a0001c0001t0036 | 2 | NA19009.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3497A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3497 | chr6 | 73504232 | |||||
chr6:73504261
|
A | C | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3526A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3526 | chr6 | 73504261 | |||||
chr6:73504283
|
C | T | 11 | a0001c0001t0003a0001c0001t0019a0001c0001t0033others(8): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3548C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3548 | chr6 | 73504283 | |||||
chr6:73504350
|
C | T | 1 | a0001c0001t0093 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3615C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3615 | chr6 | 73504350 | |||||
chr6:73504418
|
A | G | 1 | a0001c0001t0018 | 4 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3683A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3683 | chr6 | 73504418 | |||||
chr6:73504707
|
C | G | 1 | a0001c0001t0059 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3972C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3972 | chr6 | 73504707 | |||||
chr6:73504715
|
C | T | 11 | a0001c0002t0020a0001c0002t0021a0001c0002t0027others(8): Show | 23 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 3980 | chr6 | 73504715 | |||||
chr6:73504828
|
G | A | 1 | a0001c0001t0069 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4093G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4093 | chr6 | 73504828 | |||||
chr6:73504953
|
G | A | 1 | a0001c0001t0070 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4218G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4218 | chr6 | 73504953 | |||||
chr6:73505181
|
C | CA | 20 | a0001c0001t0071a0001c0002t0002a0001c0002t0011others(17): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4458dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4459 | INFO_REALIGN_3_PRIME | chr6 | 73505181 | ||||
chr6:73505194
|
T | A | 3 | a0001c0001t0025a0001c0001t0097a0001c0001t0098 | 5 | HG02622.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4459T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4459 | chr6 | 73505194 | |||||
chr6:73505256
|
G | A | 1 | a0001c0001t0051 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4521G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4521 | chr6 | 73505256 | |||||
chr6:73505320
|
G | A | 11 | a0001c0002t0020a0001c0002t0021a0001c0002t0028others(8): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4585G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4585 | chr6 | 73505320 | |||||
chr6:73505394
|
C | T | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4659C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4659 | chr6 | 73505394 | |||||
chr6:73505403
|
A | C | 1 | a0001c0001t0040 | 2 | HG00140.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4668A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4668 | chr6 | 73505403 | |||||
chr6:73505537
|
AT | A | 19 | a0001c0001t0071a0001c0002t0002a0001c0002t0011others(16): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4805delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4805 | INFO_REALIGN_3_PRIME | chr6 | 73505537 | ||||
chr6:73505551
|
GTTTTGTT others(5): Show |
G | 48 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(45): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*4828_*4839delTTTT others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4828 | INFO_REALIGN_3_PRIME | chr6 | 73505551 | ||||
chr6:73505562
|
G | A | 4 | a0001c0001t0014a0001c0001t0037a0001c0001t0095others(1): Show | 10 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4827G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4827 | chr6 | 73505562 | |||||
chr6:73505691
|
T | C | 2 | a0001c0002t0111a0001c0002t0112 | 2 | NA19011.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4956T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 4956 | chr6 | 73505691 | |||||
chr6:73505745
|
G | A | 7 | a0001c0001t0005a0001c0001t0031a0001c0001t0041others(4): Show | 24 | HG00741.hp1 HG01074.hp2 HG01257.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5010G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5010 | chr6 | 73505745 | |||||
chr6:73506134
|
A | G | 1 | a0001c0001t0109 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5399 | chr6 | 73506134 | |||||
chr6:73506293
|
T | C | 1 | a0001c0001t0097 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5558T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5558 | chr6 | 73506293 | |||||
chr6:73506478
|
G | A | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(59): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*5743G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5743 | chr6 | 73506478 | |||||
chr6:73506551
|
A | G | 17 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(14): Show | 55 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*5816A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5816 | chr6 | 73506551 | |||||
chr6:73506682
|
C | CT | 27 | a0001c0001t0043a0001c0001t0048a0001c0001t0054others(24): Show | 69 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5970dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5971 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | ||||
chr6:73506682
|
C | CTT | 9 | a0001c0001t0044a0001c0002t0029a0001c0002t0039others(6): Show | 12 | HG00438.hp2 HG01978.hp1 HG02080.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5969_*5970dupTT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5971 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | ||||
chr6:73506682
|
CT | C | 59 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(56): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*5970delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5970 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | ||||
chr6:73506682
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0004a0001c0001t0032a0001c0001t0051others(6): Show | 30 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5963_*5970delTTTT others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 5963 | INFO_REALIGN_3_PRIME | chr6 | 73506682 | ||||
chr6:73506749
|
C | T | 10 | a0001c0001t0006a0001c0001t0023a0001c0001t0024others(7): Show | 30 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6014C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6014 | chr6 | 73506749 | |||||
chr6:73506879
|
G | C | 6 | a0001c0002t0021a0001c0002t0029a0001c0002t0124others(3): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6144G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6144 | chr6 | 73506879 | |||||
chr6:73506914
|
C | CCTGACCT others(689): Show |
3 | a0001c0001t0025a0001c0001t0097a0001c0001t0099 | 5 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(688): Show |
1 | a0001c0001t0081 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(691): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(690): Show |
1 | a0001c0001t0072 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(689): Show |
46 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(43): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(689): Show |
9 | a0001c0001t0103a0001c0002t0021a0001c0002t0029others(6): Show | 14 | HG01884.hp1 HG02165.hp1 HG02273.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(689): Show |
30 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(27): Show | 95 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(689): Show |
3 | a0001c0002t0020a0001c0002t0028a0001c0002t0123 | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(692): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(690): Show |
4 | a0001c0001t0014a0001c0001t0037a0001c0001t0056others(1): Show | 10 | HG00408.hp2 HG02132.hp2 NA18612.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(690): Show |
21 | a0001c0001t0054a0001c0001t0071a0001c0001t0095others(18): Show | 59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(691): Show |
1 | a0001c0002t0116 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(694): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506914
|
C | CCTGACCT others(690): Show |
1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6199_*6200insTGCC others(693): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6200 | INFO_REALIGN_3_PRIME | chr6 | 73506914 | ||||
chr6:73506996
|
C | T | 1 | a0001c0001t0106 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6261C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6261 | chr6 | 73506996 | |||||
chr6:73507070
|
A | G | 6 | a0001c0002t0021a0001c0002t0029a0001c0002t0124others(3): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6335A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6335 | chr6 | 73507070 | |||||
chr6:73507220
|
T | G | 48 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(45): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*6485T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6485 | chr6 | 73507220 | |||||
chr6:73507385
|
A | G | 1 | a0001c0002t0118 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6650A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6650 | chr6 | 73507385 | |||||
chr6:73507547
|
G | A | 15 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(12): Show | 48 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*6812G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6812 | chr6 | 73507547 | |||||
chr6:73507555
|
G | A | 120 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(117): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*6820G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6820 | chr6 | 73507555 | |||||
chr6:73507703
|
T | C | 1 | a0001c0002t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6968T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6968 | chr6 | 73507703 | |||||
chr6:73507705
|
C | T | 1 | a0001c0001t0128 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6970 | chr6 | 73507705 | |||||
chr6:73507715
|
C | A | 28 | a0001c0001t0045a0001c0001t0054a0001c0001t0058others(25): Show | 71 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*6980C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 6980 | chr6 | 73507715 | |||||
chr6:73507793
|
T | A | 1 | a0001c0001t0055 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7058T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7058 | chr6 | 73507793 | |||||
chr6:73507793
|
T | C | 1 | a0001c0001t0084 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7058T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7058 | chr6 | 73507793 | |||||
chr6:73507801
|
C | A | 2 | a0001c0001t0046a0001c0001t0074 | 2 | NA18969.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7066C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7066 | chr6 | 73507801 | |||||
chr6:73507807
|
G | C | 3 | a0001c0001t0055a0001c0001t0068a0001c0001t0075 | 3 | HG00408.hp1 HG02015.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7072G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7072 | chr6 | 73507807 | |||||
chr6:73507837
|
T | C | 133 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(130): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*7102T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7102 | chr6 | 73507837 | |||||
chr6:73507843
|
G | A | 2 | a0001c0001t0098a0001c0001t0100 | 2 | HG03098.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7108G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7108 | chr6 | 73507843 | |||||
chr6:73507845
|
T | C | 5 | a0001c0001t0031a0001c0001t0071a0001c0001t0098others(2): Show | 6 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7110T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7110 | chr6 | 73507845 | |||||
chr6:73507847
|
C | G | 133 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(130): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*7112C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7112 | chr6 | 73507847 | |||||
chr6:73507869
|
C | T | 1 | a0001c0001t0068 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7134C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7134 | chr6 | 73507869 | |||||
chr6:73507894
|
G | A | 1 | a0001c0001t0085 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7159G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7159 | chr6 | 73507894 | |||||
chr6:73507932
|
G | A | 3 | a0001c0001t0019a0001c0001t0053a0001c0001t0107 | 6 | HG02004.hp2 HG02273.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7197G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7197 | chr6 | 73507932 | |||||
chr6:73507933
|
C | T | 3 | a0001c0001t0019a0001c0001t0053a0001c0001t0107 | 6 | HG02004.hp2 HG02273.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7198C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7198 | chr6 | 73507933 | |||||
chr6:73507946
|
T | C | 1 | a0001c0001t0082 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7211T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7211 | chr6 | 73507946 | |||||
chr6:73507956
|
G | T | 1 | a0001c0002t0127 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7221G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7221 | chr6 | 73507956 | |||||
chr6:73507976
|
CA | C | 28 | a0001c0001t0008a0001c0001t0025a0001c0001t0045others(25): Show | 72 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*7265delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7265 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | ||||
chr6:73507976
|
CAA | C | 23 | a0001c0001t0007a0001c0001t0016a0001c0001t0024others(20): Show | 50 | HG00280.hp2 HG01516.hp2 HG01884.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*7264_*7265delAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7264 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | ||||
chr6:73507976
|
CAAA | C | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(64): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*7263_*7265delAAA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7263 | INFO_REALIGN_3_PRIME | chr6 | 73507976 | ||||
chr6:73508101
|
T | A | 1 | a0001c0002t0123 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7366T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7366 | chr6 | 73508101 | |||||
chr6:73508210
|
T | C | 1 | a0001c0001t0043 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7475T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7475 | chr6 | 73508210 | |||||
chr6:73508311
|
T | C | 1 | a0001c0001t0079 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7576T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7576 | chr6 | 73508311 | |||||
chr6:73508418
|
T | C | 2 | a0001c0001t0077a0001c0001t0087 | 2 | HG03710.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7683T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7683 | chr6 | 73508418 | |||||
chr6:73508482
|
A | T | 1 | a0001c0001t0076 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7747A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7747 | chr6 | 73508482 | |||||
chr6:73508557
|
A | C | 10 | a0001c0001t0016a0001c0001t0025a0001c0001t0047others(7): Show | 22 | HG02257.hp1 HG02622.hp2 HG02647.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7822A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7822 | chr6 | 73508557 | |||||
chr6:73508573
|
A | G | 1 | a0001c0002t0027 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7838A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7838 | chr6 | 73508573 | |||||
chr6:73508671
|
G | C | 2 | a0001c0001t0078a0001c0001t0080 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7936G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 7936 | chr6 | 73508671 | |||||
chr6:73509040
|
A | T | 4 | a0001c0001t0047a0001c0002t0020a0001c0002t0028others(1): Show | 9 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8305A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 12/12 | 8305 | chr6 | 73509040 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:73462271
|
A | G | 1 | a0001c0002t0118g0368 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.217+200A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462271 | ||||||
chr6:73462331
|
C | T | 3 | a0001c0001t0016g0366a0001c0001t0016g0367a0001c0002t0112g0365 | 3 | NA18957.hp1 NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.217+260C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462331 | ||||||
chr6:73462344
|
G | GAGA | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+273_217+274ins others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462344 | ||||||
chr6:73462347
|
A | T | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+276A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462347 | ||||||
chr6:73462349
|
C | A | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+278C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462349 | ||||||
chr6:73462350
|
A | AG | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+279_217+280ins others(1): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462350 | ||||||
chr6:73462352
|
C | A | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.217+281C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462352 | ||||||
chr6:73462624
|
G | C | 5 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0366others(2): Show | 5 | NA18946.hp2 NA18957.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+553G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462624 | ||||||
chr6:73462654
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.217+583G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462654 | ||||||
chr6:73462664
|
G | A | 55 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.217+593G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462664 | ||||||
chr6:73462684
|
C | G | 1 | a0001c0002t0119g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.217+613C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462684 | ||||||
chr6:73462753
|
A | T | 7 | a0001c0002t0021g0087a0001c0002t0021g0089a0001c0002t0027g0090others(4): Show | 7 | HG01109.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+682A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462753 | ||||||
chr6:73462798
|
A | G | 1 | a0001c0002t0002g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.217+727A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462798 | ||||||
chr6:73462863
|
G | A | 55 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.217+792G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462863 | ||||||
chr6:73462867
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0122 | 3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.217+796G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73462867 | ||||||
chr6:73463000
|
T | C | 337 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(334): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.217+929T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463000 | ||||||
chr6:73463008
|
G | A | 1 | a0001c0001t0012g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+937G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463008 | ||||||
chr6:73463020
|
C | CT | 9 | a0001c0001t0001g0326a0001c0001t0005g0364a0001c0001t0007g0325others(6): Show | 9 | HG02615.hp1 HG02738.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+965dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73463020 | |||||
chr6:73463020
|
CTTT | C | 32 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(29): Show | 37 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+963_217+965del others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73463020 | |||||
chr6:73463273
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.217+1202C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463273 | ||||||
chr6:73463292
|
A | G | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.217+1221A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463292 | ||||||
chr6:73463333
|
A | G | 1 | a0001c0001t0006g0323 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.217+1262A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463333 | ||||||
chr6:73463709
|
T | C | 5 | a0001c0001t0009g0126a0001c0001t0009g0127a0001c0001t0009g0128others(2): Show | 5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+1638T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463709 | ||||||
chr6:73463833
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.217+1762C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463833 | ||||||
chr6:73463951
|
G | A | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.217+1880G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73463951 | ||||||
chr6:73464296
|
C | G | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0122 | 3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.218-1913C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464296 | ||||||
chr6:73464402
|
C | T | 3 | a0001c0001t0032g0322a0001c0001t0056g0320a0001c0001t0059g0321 | 3 | NA18965.hp2 NA18999.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.218-1807C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464402 | ||||||
chr6:73464441
|
A | G | 1 | a0001c0001t0098g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218-1768A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464441 | ||||||
chr6:73464638
|
C | T | 77 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(74): Show | 77 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.218-1571C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464638 | ||||||
chr6:73464659
|
T | TA | 13 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(10): Show | 16 | HG01891.hp1 HG02056.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-1533dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464659 | |||||
chr6:73464659
|
TA | T | 29 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(26): Show | 29 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-1533delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464659 | |||||
chr6:73464671
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-1538A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464671 | ||||||
chr6:73464673
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0007g0315 | 2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.218-1536A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464673 | ||||||
chr6:73464790
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.218-1419G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464790 | ||||||
chr6:73464801
|
C | T | 4 | a0001c0002t0021g0087a0001c0002t0021g0089a0001c0002t0125g0086others(1): Show | 4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-1408C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464801 | ||||||
chr6:73464803
|
C | A | 1 | a0001c0001t0003g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.218-1406C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464803 | ||||||
chr6:73464826
|
ACT | A | 12 | a0001c0002t0021g0080a0001c0002t0021g0087a0001c0002t0021g0089others(9): Show | 12 | HG02165.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.218-1380_218-1379d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464826 | |||||
chr6:73464835
|
C | CA | 90 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0165others(87): Show | 92 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.218-1348dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | |||||
chr6:73464835
|
C | CAA | 13 | a0001c0001t0001g0136a0001c0001t0007g0145a0001c0001t0007g0146others(10): Show | 13 | HG00280.hp1 HG00280.hp2 HG03471.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-1349_218-1348d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | |||||
chr6:73464835
|
C | CAAA | 8 | a0001c0001t0025g0140a0001c0001t0025g0141a0001c0001t0025g0142others(5): Show | 8 | HG01358.hp2 HG02027.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-1350_218-1348d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | |||||
chr6:73464835
|
CA | C | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0005g0364others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-1348delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464835 | |||||
chr6:73464846
|
A | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218-1363A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464846 | ||||||
chr6:73464859
|
A | AAC | 9 | a0001c0002t0020g0072a0001c0002t0021g0080a0001c0002t0028g0074others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.218-1349_218-1348i others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 73464859 | |||||
chr6:73464859
|
A | AC | 18 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0027others(15): Show | 18 | HG00438.hp2 HG01261.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-1350_218-1349i others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464859 | ||||||
chr6:73464859
|
A | C | 53 | a0001c0002t0002g0007a0001c0002t0002g0034a0001c0002t0002g0035others(50): Show | 53 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.218-1350A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464859 | ||||||
chr6:73464994
|
A | G | 2 | a0001c0001t0005g0364a0001c0001t0042g0363 | 2 | NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.218-1215A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73464994 | ||||||
chr6:73465218
|
C | T | 1 | a0001c0001t0015g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.218-991C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465218 | ||||||
chr6:73465276
|
G | A | 1 | a0001c0001t0099g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.218-933G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465276 | ||||||
chr6:73465403
|
A | G | 1 | a0001c0001t0003g0114 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.218-806A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465403 | ||||||
chr6:73465443
|
C | T | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-766C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465443 | ||||||
chr6:73465459
|
C | T | 20 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(17): Show | 20 | HG02165.hp1 HG02257.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.218-750C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465459 | ||||||
chr6:73465469
|
T | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0158others(89): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.218-740T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465469 | ||||||
chr6:73465611
|
T | A | 1 | a0001c0002t0002g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.218-598T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465611 | ||||||
chr6:73465715
|
G | A | 1 | a0001c0002t0011g0029 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.218-494G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465715 | ||||||
chr6:73465869
|
G | A | 337 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(334): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.218-340G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465869 | ||||||
chr6:73465899
|
G | A | 1 | a0001c0001t0054g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.218-310G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73465899 | ||||||
chr6:73466171
|
G | A | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.218-38G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 1/11 | chr6 | 73466171 | ||||||
chr6:73466658
|
G | A | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+52G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73466658 | ||||||
chr6:73466946
|
TTATA | T | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.535+346_535+349del others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73466946 | |||||
chr6:73466997
|
TC | T | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+392delC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73466997 | ||||||
chr6:73467124
|
G | A | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+518G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467124 | ||||||
chr6:73467144
|
T | C | 3 | a0001c0001t0025g0140a0001c0001t0025g0141a0001c0001t0025g0142 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.535+538T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467144 | ||||||
chr6:73467263
|
G | A | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.535+657G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467263 | ||||||
chr6:73467614
|
A | AAAAT | 95 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(92): Show | 102 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.535+1034_535+1037d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467614
|
A | AAAATAAA others(1): Show |
119 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.535+1030_535+1037d others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467614
|
A | AAAATAAA others(5): Show |
53 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0191others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.535+1026_535+1037d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467614
|
A | AAAATAAA others(9): Show |
27 | a0001c0001t0006g0249a0001c0001t0025g0141a0001c0001t0025g0142others(24): Show | 27 | HG01070.hp2 HG01099.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.535+1022_535+1037d others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467614
|
A | AAAATAAA others(13): Show |
36 | a0001c0001t0025g0140a0001c0002t0002g0025a0001c0002t0002g0026others(33): Show | 36 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+1018_535+1037d others(22): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467614
|
A | AAAATAAA others(17): Show |
5 | a0001c0002t0011g0022a0001c0002t0011g0031a0001c0002t0038g0030others(2): Show | 5 | HG00438.hp2 HG01261.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+1014_535+1037d others(26): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467614 | |||||
chr6:73467615
|
A | AAATAAAT others(12): Show |
1 | a0001c0001t0099g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.535+1012_535+1030d others(21): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73467615 | |||||
chr6:73467786
|
G | A | 1 | a0001c0001t0100g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.535+1180G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467786 | ||||||
chr6:73467796
|
T | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1190T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467796 | ||||||
chr6:73467888
|
T | A | 1 | a0001c0001t0078g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.535+1282T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467888 | ||||||
chr6:73467924
|
G | A | 13 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(10): Show | 13 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+1318G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467924 | ||||||
chr6:73467968
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1362G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73467968 | ||||||
chr6:73468036
|
G | A | 1 | a0002c0009t0010g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.535+1430G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468036 | ||||||
chr6:73468043
|
T | A | 1 | a0001c0001t0003g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.535+1437T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468043 | ||||||
chr6:73468065
|
C | T | 21 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(18): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.535+1459C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468065 | ||||||
chr6:73468108
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+1502C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468108 | ||||||
chr6:73468143
|
A | G | 4 | a0001c0002t0021g0087a0001c0002t0021g0089a0001c0002t0125g0086others(1): Show | 4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+1537A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468143 | ||||||
chr6:73468224
|
T | C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.535+1618T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468224 | ||||||
chr6:73468321
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.535+1715G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468321 | ||||||
chr6:73468365
|
C | T | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.535+1759C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468365 | ||||||
chr6:73468397
|
G | C | 1 | a0001c0002t0021g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.535+1791G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468397 | ||||||
chr6:73468673
|
T | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+2067T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468673 | ||||||
chr6:73468851
|
G | A | 11 | a0001c0001t0008g0019a0001c0001t0008g0120a0001c0001t0008g0121others(8): Show | 11 | HG02040.hp2 HG02055.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+2245G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468851 | ||||||
chr6:73468917
|
T | C | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.535+2311T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468917 | ||||||
chr6:73468989
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.535+2383T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73468989 | ||||||
chr6:73469001
|
T | C | 10 | a0001c0001t0001g0158a0001c0001t0001g0310a0001c0001t0007g0145others(7): Show | 10 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.535+2395T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469001 | ||||||
chr6:73469123
|
A | G | 1 | a0001c0002t0002g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.535+2517A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469123 | ||||||
chr6:73469191
|
C | T | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.535+2585C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469191 | ||||||
chr6:73469192
|
G | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+2586G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469192 | ||||||
chr6:73469377
|
C | T | 1 | a0001c0001t0004g0210 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.535+2771C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469377 | ||||||
chr6:73469440
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.535+2834A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469440 | ||||||
chr6:73469441
|
T | C | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.535+2835T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469441 | ||||||
chr6:73469483
|
G | A | 8 | a0001c0001t0004g0200a0001c0001t0004g0276a0001c0001t0004g0277others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+2877G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469483 | ||||||
chr6:73469499
|
G | C | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+2893G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469499 | ||||||
chr6:73469529
|
A | G | 1 | a0001c0001t0032g0322 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.535+2923A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469529 | ||||||
chr6:73469536
|
C | T | 1 | a0001c0001t0006g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.535+2930C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469536 | ||||||
chr6:73469598
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.535+2992G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469598 | ||||||
chr6:73469650
|
CT | C | 337 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(334): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.535+3046delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73469650 | |||||
chr6:73469672
|
A | G | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.535+3066A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469672 | ||||||
chr6:73469803
|
G | C | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.535+3197G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469803 | ||||||
chr6:73469890
|
A | C | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+3284A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469890 | ||||||
chr6:73469965
|
A | T | 19 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0001g0182others(16): Show | 20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.535+3359A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73469965 | ||||||
chr6:73470053
|
A | G | 2 | a0001c0001t0013g0183a0001c0001t0013g0184 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.536-3312A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470053 | ||||||
chr6:73470065
|
G | A | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.536-3300G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470065 | ||||||
chr6:73470084
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0001g0131others(8): Show | 12 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.536-3281A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470084 | ||||||
chr6:73470202
|
A | AT | 4 | a0001c0001t0018g0144a0001c0001t0018g0147a0001c0001t0018g0159others(1): Show | 4 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-3157dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73470202 | |||||
chr6:73470261
|
C | T | 1 | a0001c0002t0116g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.536-3104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470261 | ||||||
chr6:73470268
|
G | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-3097G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470268 | ||||||
chr6:73470302
|
G | A | 1 | a0001c0001t0008g0330 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.536-3063G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470302 | ||||||
chr6:73470310
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-3055G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470310 | ||||||
chr6:73470345
|
T | C | 8 | a0001c0001t0003g0106a0001c0001t0003g0117a0001c0001t0003g0118others(5): Show | 8 | HG02004.hp2 HG02273.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-3020T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470345 | ||||||
chr6:73470393
|
A | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-2972A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470393 | ||||||
chr6:73470453
|
A | G | 3 | a0001c0002t0002g0052a0001c0002t0002g0053a0001c0002t0011g0029 | 3 | HG02056.hp1 NA18987.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.536-2912A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470453 | ||||||
chr6:73470469
|
G | A | 3 | a0001c0001t0025g0140a0001c0001t0025g0141a0001c0001t0025g0142 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.536-2896G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470469 | ||||||
chr6:73470474
|
G | A | 1 | a0001c0001t0049g0341 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-2891G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470474 | ||||||
chr6:73470479
|
T | C | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.536-2886T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470479 | ||||||
chr6:73470498
|
G | A | 8 | a0001c0001t0014g0013a0001c0001t0014g0285a0001c0001t0014g0286others(5): Show | 8 | HG00408.hp2 NA18612.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-2867G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470498 | ||||||
chr6:73470500
|
G | A | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.536-2865G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470500 | ||||||
chr6:73470530
|
A | G | 1 | a0001c0001t0061g0300 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.536-2835A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470530 | ||||||
chr6:73470620
|
C | G | 3 | a0001c0001t0025g0140a0001c0001t0025g0141a0001c0001t0025g0142 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.536-2745C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470620 | ||||||
chr6:73470689
|
C | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-2676C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470689 | ||||||
chr6:73470881
|
A | T | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.536-2484A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470881 | ||||||
chr6:73470918
|
A | T | 1 | a0001c0001t0025g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.536-2447A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73470918 | ||||||
chr6:73471006
|
A | T | 1 | a0001c0001t0098g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.536-2359A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471006 | ||||||
chr6:73471086
|
A | G | 21 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(18): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-2279A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471086 | ||||||
chr6:73471121
|
C | T | 21 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(18): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-2244C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471121 | ||||||
chr6:73471122
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.536-2243G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471122 | ||||||
chr6:73471206
|
C | CT | 319 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(316): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.536-2148dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73471206 | |||||
chr6:73471252
|
A | G | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.536-2113A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471252 | ||||||
chr6:73471471
|
G | A | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.536-1894G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471471 | ||||||
chr6:73471658
|
T | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.536-1707T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471658 | ||||||
chr6:73471681
|
G | T | 2 | a0001c0002t0021g0071a0001c0002t0021g0080 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.536-1684G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471681 | ||||||
chr6:73471717
|
C | T | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.536-1648C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471717 | ||||||
chr6:73471718
|
G | A | 3 | a0001c0001t0001g0267a0001c0001t0007g0196a0001c0001t0007g0312 | 3 | HG02280.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.536-1647G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471718 | ||||||
chr6:73471771
|
G | A | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-1594G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471771 | ||||||
chr6:73471818
|
ATG | A | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1545_536-1544d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73471818 | |||||
chr6:73471856
|
G | A | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1509G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471856 | ||||||
chr6:73471899
|
C | T | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.536-1466C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73471899 | ||||||
chr6:73472009
|
TG | T | 199 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(196): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.536-1355delG | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472009 | ||||||
chr6:73472027
|
G | A | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.536-1338G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472027 | ||||||
chr6:73472127
|
G | A | 2 | a0001c0002t0011g0054a0001c0002t0038g0032 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.536-1238G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472127 | ||||||
chr6:73472159
|
T | C | 1 | a0001c0001t0045g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-1206T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472159 | ||||||
chr6:73472202
|
G | A | 1 | a0001c0002t0002g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.536-1163G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472202 | ||||||
chr6:73472425
|
GACTA | G | 5 | a0001c0001t0009g0126a0001c0001t0009g0127a0001c0001t0009g0128others(2): Show | 5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.536-936_536-933del others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73472425 | |||||
chr6:73472525
|
A | G | 2 | a0001c0002t0121g0081a0001c0002t0122g0085 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.536-840A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472525 | ||||||
chr6:73472716
|
C | CA | 152 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.536-648dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73472716 | |||||
chr6:73472729
|
G | A | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.536-636G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472729 | ||||||
chr6:73472843
|
A | G | 21 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(18): Show | 21 | HG01884.hp1 HG02165.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.536-522A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472843 | ||||||
chr6:73472939
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.536-426G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73472939 | ||||||
chr6:73473003
|
C | T | 2 | a0001c0002t0121g0081a0001c0002t0122g0085 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.536-362C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473003 | ||||||
chr6:73473182
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.536-183G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473182 | ||||||
chr6:73473210
|
C | T | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.536-155C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | chr6 | 73473210 | ||||||
chr6:73473277
|
C | CAGAT | 22 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0004g0299others(19): Show | 23 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.536-66_536-63dupGA others(2): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | |||||
chr6:73473277
|
C | CAGATAGA others(5): Show |
1 | a0001c0001t0001g0182 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.536-74_536-63dupGA others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | |||||
chr6:73473277
|
CAGAT | C | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.536-66_536-63delGA others(2): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 73473277 | |||||
chr6:73473721
|
C | CT | 292 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0131others(289): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.825+84dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473721 | |||||
chr6:73473761
|
C | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.825+107C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473761 | ||||||
chr6:73473768
|
T | C | 1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.825+114T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473768 | ||||||
chr6:73473786
|
A | AT | 30 | a0001c0001t0001g0245a0001c0001t0001g0274a0001c0001t0003g0002others(27): Show | 32 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.825+150dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473786 | |||||
chr6:73473786
|
AT | A | 73 | a0001c0001t0013g0176a0001c0001t0016g0094a0001c0001t0016g0185others(70): Show | 73 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.825+150delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73473786 | |||||
chr6:73473861
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0239others(4): Show | 9 | HG02129.hp1 NA18939.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.825+207A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73473861 | ||||||
chr6:73474098
|
C | CT | 8 | a0001c0001t0004g0210a0001c0001t0005g0355a0001c0001t0010g0016others(5): Show | 9 | HG01123.hp1 HG01346.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.825+456dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73474098 | |||||
chr6:73474112
|
T | A | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.825+458T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474112 | ||||||
chr6:73474592
|
G | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0113a0001c0001t0003g0114 | 3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+938G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474592 | ||||||
chr6:73474593
|
C | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0113a0001c0001t0003g0114 | 3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+939C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474593 | ||||||
chr6:73474594
|
A | C | 1 | a0001c0001t0009g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.825+940A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474594 | ||||||
chr6:73474594
|
ACCC | A | 3 | a0001c0001t0003g0104a0001c0001t0003g0113a0001c0001t0003g0114 | 3 | NA18980.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.825+941_825+943del others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474594 | ||||||
chr6:73474691
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.825+1037G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474691 | ||||||
chr6:73474752
|
CT | C | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.825+1110delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73474752 | |||||
chr6:73474777
|
C | T | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.825+1123C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474777 | ||||||
chr6:73474786
|
G | A | 4 | a0001c0002t0021g0087a0001c0002t0021g0089a0001c0002t0125g0086others(1): Show | 4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.825+1132G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474786 | ||||||
chr6:73474812
|
A | G | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.825+1158A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474812 | ||||||
chr6:73474817
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.825+1163G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474817 | ||||||
chr6:73474856
|
A | G | 1 | a0001c0001t0007g0155 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.825+1202A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474856 | ||||||
chr6:73474907
|
C | T | 1 | a0001c0001t0006g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.825+1253C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73474907 | ||||||
chr6:73475114
|
A | G | 1 | a0001c0001t0013g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.825+1460A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475114 | ||||||
chr6:73475183
|
G | C | 1 | a0001c0001t0045g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.825+1529G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475183 | ||||||
chr6:73475249
|
G | A | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.825+1595G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475249 | ||||||
chr6:73475259
|
G | T | 1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.825+1605G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475259 | ||||||
chr6:73475369
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.825+1715G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475369 | ||||||
chr6:73475434
|
C | T | 3 | a0001c0002t0002g0050a0001c0002t0002g0066a0001c0002t0011g0061 | 3 | NA18959.hp1 NA18981.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.825+1780C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475434 | ||||||
chr6:73475496
|
A | G | 7 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(4): Show | 7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.825+1842A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475496 | ||||||
chr6:73475512
|
C | CT | 11 | a0001c0001t0009g0238a0001c0001t0024g0263a0001c0001t0085g0171others(8): Show | 11 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.825+1873dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73475512 | |||||
chr6:73475528
|
C | T | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.825+1874C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475528 | ||||||
chr6:73475529
|
T | C | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.825+1875T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475529 | ||||||
chr6:73475567
|
C | T | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.825+1913C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475567 | ||||||
chr6:73475627
|
G | A | 2 | a0001c0002t0121g0081a0001c0002t0122g0085 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.825+1973G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475627 | ||||||
chr6:73475659
|
C | T | 1 | a0001c0001t0006g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.825+2005C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475659 | ||||||
chr6:73475687
|
T | C | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.825+2033T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475687 | ||||||
chr6:73475702
|
G | C | 1 | a0001c0001t0017g0357 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.825+2048G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475702 | ||||||
chr6:73475751
|
A | T | 1 | a0001c0001t0071g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.825+2097A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475751 | ||||||
chr6:73475758
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.825+2104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475758 | ||||||
chr6:73475764
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.825+2110G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475764 | ||||||
chr6:73475793
|
T | G | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.825+2139T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475793 | ||||||
chr6:73475826
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.825+2172G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475826 | ||||||
chr6:73475944
|
C | T | 1 | a0001c0001t0009g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.825+2290C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475944 | ||||||
chr6:73475947
|
C | A | 1 | a0001c0001t0008g0346 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.825+2293C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475947 | ||||||
chr6:73475965
|
A | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.825+2311A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73475965 | ||||||
chr6:73476088
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0007g0146 | 2 | NA19001.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.825+2434C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476088 | ||||||
chr6:73476134
|
A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.825+2480A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476134 | ||||||
chr6:73476203
|
A | AAATAAAA others(7): Show |
57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.825+2552_825+2565d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476203 | |||||
chr6:73476222
|
A | C | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.825+2568A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476222 | ||||||
chr6:73476285
|
A | G | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0122 | 3 | HG02040.hp2 HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.825+2631A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476285 | ||||||
chr6:73476378
|
C | CA | 11 | a0001c0001t0004g0203a0001c0001t0008g0346a0001c0001t0016g0094others(8): Show | 11 | HG00280.hp1 HG00673.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.825+2743dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | |||||
chr6:73476378
|
CA | C | 59 | a0001c0001t0001g0243a0001c0001t0003g0118a0001c0001t0005g0352others(56): Show | 59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.825+2743delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | |||||
chr6:73476378
|
CAA | C | 23 | a0001c0002t0002g0049a0001c0002t0002g0053a0001c0002t0020g0072others(20): Show | 23 | HG01515.hp2 HG01884.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.825+2742_825+2743d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476378 | |||||
chr6:73476440
|
G | A | 1 | a0001c0002t0120g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.825+2786G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476440 | ||||||
chr6:73476452
|
A | AAAG | 80 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(77): Show | 80 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.825+2800_825+2801i others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476452 | |||||
chr6:73476572
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0035g0135 | 3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.825+2918G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476572 | ||||||
chr6:73476739
|
C | A | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.826-2993C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476739 | ||||||
chr6:73476790
|
A | AT | 18 | a0001c0001t0016g0093a0001c0001t0016g0185a0001c0001t0016g0186others(15): Show | 18 | HG02572.hp2 HG02622.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.826-2926dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476790 | |||||
chr6:73476790
|
AT | A | 9 | a0001c0001t0003g0118a0001c0001t0006g0251a0001c0001t0058g0288others(6): Show | 9 | HG01109.hp2 HG01256.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.826-2926delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73476790 | |||||
chr6:73476812
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.826-2920G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476812 | ||||||
chr6:73476912
|
T | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.826-2820T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476912 | ||||||
chr6:73476920
|
C | T | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.826-2812C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476920 | ||||||
chr6:73476943
|
A | G | 1 | a0001c0001t0005g0362 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.826-2789A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73476943 | ||||||
chr6:73477079
|
G | A | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826-2653G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477079 | ||||||
chr6:73477093
|
T | A | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.826-2639T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477093 | ||||||
chr6:73477257
|
A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.826-2475A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477257 | ||||||
chr6:73477393
|
CA | C | 182 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0134others(179): Show | 185 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.826-2317delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477393 | |||||
chr6:73477393
|
CAA | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.826-2318_826-2317d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477393 | |||||
chr6:73477395
|
A | AAAAAAAA others(844): Show |
1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.826-2319_826-2318i others(853): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477395 | |||||
chr6:73477411
|
A | G | 1 | a0001c0001t0098g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826-2321A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477411 | ||||||
chr6:73477509
|
C | CT | 17 | a0001c0001t0001g0236a0001c0001t0008g0340a0001c0001t0015g0297others(14): Show | 17 | HG00621.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.826-2208dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73477509 | |||||
chr6:73477633
|
A | G | 1 | a0001c0002t0002g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.826-2099A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477633 | ||||||
chr6:73477767
|
A | G | 22 | a0001c0002t0002g0026a0001c0002t0002g0027a0001c0002t0002g0041others(19): Show | 22 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.826-1965A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477767 | ||||||
chr6:73477799
|
G | A | 1 | a0001c0001t0098g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826-1933G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477799 | ||||||
chr6:73477817
|
T | G | 1 | a0001c0002t0021g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.826-1915T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477817 | ||||||
chr6:73477848
|
G | A | 1 | a0001c0001t0045g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.826-1884G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477848 | ||||||
chr6:73477944
|
T | C | 1 | a0001c0001t0012g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.826-1788T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73477944 | ||||||
chr6:73478108
|
G | A | 1 | a0001c0002t0002g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.826-1624G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478108 | ||||||
chr6:73478244
|
CA | C | 71 | a0001c0001t0032g0296a0001c0002t0002g0007a0001c0002t0002g0025others(68): Show | 71 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.826-1472delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478244 | |||||
chr6:73478345
|
C | A | 1 | a0002c0009t0010g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826-1387C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478345 | ||||||
chr6:73478347
|
A | G | 2 | a0001c0001t0008g0330a0001c0001t0048g0339 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.826-1385A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478347 | ||||||
chr6:73478416
|
C | CA | 63 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(60): Show | 65 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.826-1306dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478416 | |||||
chr6:73478482
|
T | G | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.826-1250T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478482 | ||||||
chr6:73478629
|
C | G | 1 | a0001c0002t0027g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.826-1103C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478629 | ||||||
chr6:73478789
|
A | G | 343 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(340): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.826-943A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478789 | ||||||
chr6:73478880
|
CT | C | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.826-841delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 73478880 | |||||
chr6:73478901
|
T | C | 3 | a0001c0001t0006g0188a0001c0001t0006g0252a0001c0001t0088g0189 | 3 | HG01515.hp1 HG01517.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.826-831T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478901 | ||||||
chr6:73478942
|
G | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0269a0001c0001t0009g0198 | 3 | HG02109.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.826-790G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73478942 | ||||||
chr6:73479029
|
C | T | 1 | a0001c0001t0009g0304 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.826-703C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479029 | ||||||
chr6:73479202
|
A | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0009g0304others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-530A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479202 | ||||||
chr6:73479409
|
C | T | 1 | a0001c0001t0013g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.826-323C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479409 | ||||||
chr6:73479451
|
C | T | 1 | a0001c0001t0004g0201 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.826-281C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479451 | ||||||
chr6:73479490
|
G | A | 1 | a0001c0001t0007g0145 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.826-242G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 4/11 | chr6 | 73479490 | ||||||
chr6:73480227
|
G | T | 1 | a0001c0001t0007g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1129+101G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480227 | ||||||
chr6:73480265
|
T | G | 1 | a0001c0001t0092g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1129+139T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480265 | ||||||
chr6:73480517
|
G | A | 2 | a0001c0001t0008g0120a0001c0001t0008g0121 | 2 | HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1130-158G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480517 | ||||||
chr6:73480528
|
C | G | 3 | a0001c0001t0034g0138a0001c0001t0034g0149a0001c0001t0065g0152 | 3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1130-147C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480528 | ||||||
chr6:73480548
|
G | A | 1 | a0006c0008t0001g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1130-127G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 6/11 | chr6 | 73480548 | ||||||
chr6:73480904
|
A | G | 1 | a0001c0001t0053g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1260+99A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73480904 | ||||||
chr6:73480969
|
GT | G | 46 | a0001c0001t0001g0130a0001c0001t0001g0199a0001c0001t0001g0234others(43): Show | 47 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1260+188delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73480969
|
GTT | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0131others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1260+187_1260+188d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73480969
|
GTTT | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(28): Show | 36 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260+186_1260+188d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73480969
|
GTTTT | G | 17 | a0001c0002t0002g0026a0001c0002t0002g0027a0001c0002t0002g0060others(14): Show | 17 | HG00438.hp2 HG01884.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1260+185_1260+188d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73480969
|
GTTTTT | G | 59 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0034others(56): Show | 59 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1260+184_1260+188d others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73480969
|
GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0017g0336a0001c0001t0017g0357a0001c0001t0017g0361 | 3 | HG02970.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1260+179_1260+188d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73480969 | |||||
chr6:73481161
|
C | T | 1 | a0001c0001t0075g0231 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1260+356C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481161 | ||||||
chr6:73481258
|
A | G | 7 | a0001c0001t0008g0019a0001c0001t0008g0330a0001c0001t0008g0331others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+453A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481258 | ||||||
chr6:73481306
|
G | C | 1 | a0001c0001t0004g0276 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1260+501G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481306 | ||||||
chr6:73481384
|
A | G | 25 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(22): Show | 30 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+579A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481384 | ||||||
chr6:73481468
|
TA | T | 378 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(375): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1261-564delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr6 | 73481468 | |||||
chr6:73481563
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1261-477C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481563 | ||||||
chr6:73481733
|
A | G | 4 | a0001c0002t0021g0087a0001c0002t0021g0089a0001c0002t0125g0086others(1): Show | 4 | HG02572.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-307A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481733 | ||||||
chr6:73481822
|
G | A | 343 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(340): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1261-218G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481822 | ||||||
chr6:73481864
|
A | G | 1 | a0001c0001t0044g0356 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-176A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 7/11 | chr6 | 73481864 | ||||||
chr6:73482296
|
A | G | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1465+52A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/11 | chr6 | 73482296 | ||||||
chr6:73482415
|
A | G | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1466-34A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 8/11 | chr6 | 73482415 | ||||||
chr6:73482679
|
C | A | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+59C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482679 | ||||||
chr6:73482699
|
T | G | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1637+79T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482699 | ||||||
chr6:73482789
|
C | CT | 140 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(137): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1637+191dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | |||||
chr6:73482789
|
C | CTT | 106 | a0001c0001t0001g0199a0001c0001t0001g0235a0001c0001t0001g0236others(103): Show | 111 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(108): Show |
intron_variant | MODIFIER | c.1637+190_1637+191d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | |||||
chr6:73482789
|
C | CTTT | 7 | a0001c0001t0003g0098a0001c0002t0002g0038a0001c0002t0002g0048others(4): Show | 7 | HG00438.hp2 HG00597.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+189_1637+191d others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | |||||
chr6:73482789
|
CTT | C | 11 | a0001c0001t0001g0158a0001c0001t0001g0310a0001c0001t0007g0145others(8): Show | 11 | HG00597.hp1 HG02074.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1637+190_1637+191d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | |||||
chr6:73482789
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0005g0333 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1637+178_1637+191d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73482789 | |||||
chr6:73482793
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1637+173T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482793 | ||||||
chr6:73482822
|
C | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1637+202C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482822 | ||||||
chr6:73482834
|
C | T | 1 | a0001c0001t0087g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1637+214C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482834 | ||||||
chr6:73482902
|
C | A | 1 | a0001c0002t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1637+282C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482902 | ||||||
chr6:73482937
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+317G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73482937 | ||||||
chr6:73483002
|
C | T | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+382C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483002 | ||||||
chr6:73483087
|
C | T | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+467C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483087 | ||||||
chr6:73483183
|
C | T | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1637+563C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483183 | ||||||
chr6:73483266
|
G | A | 7 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(4): Show | 7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1637+646G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483266 | ||||||
chr6:73483331
|
C | T | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1637+711C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483331 | ||||||
chr6:73483398
|
C | T | 1 | a0001c0002t0002g0047 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1637+778C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483398 | ||||||
chr6:73483464
|
A | T | 1 | a0001c0002t0011g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1637+844A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483464 | ||||||
chr6:73483506
|
A | G | 1 | a0001c0002t0122g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1637+886A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483506 | ||||||
chr6:73483654
|
C | T | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1637+1034C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483654 | ||||||
chr6:73483784
|
A | AT | 43 | a0001c0001t0001g0234a0001c0001t0003g0001a0001c0001t0003g0002others(40): Show | 48 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1637+1184dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73483784 | |||||
chr6:73483784
|
AT | A | 90 | a0001c0001t0006g0258a0001c0001t0007g0155a0001c0001t0007g0232others(87): Show | 90 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1637+1184delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73483784 | |||||
chr6:73483846
|
T | C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1637+1226T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483846 | ||||||
chr6:73483897
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1637+1277G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483897 | ||||||
chr6:73483939
|
C | T | 1 | a0001c0001t0008g0331 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1637+1319C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73483939 | ||||||
chr6:73484022
|
A | G | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+1402A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484022 | ||||||
chr6:73484101
|
T | C | 10 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(7): Show | 10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1637+1481T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484101 | ||||||
chr6:73484146
|
A | G | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1637+1526A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484146 | ||||||
chr6:73484173
|
G | A | 1 | a0001c0001t0071g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1637+1553G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484173 | ||||||
chr6:73484234
|
G | A | 2 | a0001c0001t0031g0347a0001c0001t0031g0351 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1637+1614G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484234 | ||||||
chr6:73484394
|
C | G | 2 | a0001c0002t0021g0071a0001c0002t0021g0080 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1637+1774C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484394 | ||||||
chr6:73484483
|
T | C | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1637+1863T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484483 | ||||||
chr6:73484488
|
G | A | 1 | a0001c0001t0056g0320 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1637+1868G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484488 | ||||||
chr6:73484551
|
CATT | C | 19 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0001g0182others(16): Show | 20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1637+1933_1637+193 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73484551 | |||||
chr6:73484783
|
C | T | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+2163C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484783 | ||||||
chr6:73484858
|
C | G | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1637+2238C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484858 | ||||||
chr6:73484936
|
A | C | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1637+2316A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484936 | ||||||
chr6:73484938
|
T | G | 2 | a0001c0001t0001g0163a0001c0001t0007g0148 | 2 | HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1637+2318T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484938 | ||||||
chr6:73484940
|
A | G | 1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1637+2320A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73484940 | ||||||
chr6:73485014
|
T | C | 1 | a0001c0001t0055g0290 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1637+2394T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485014 | ||||||
chr6:73485023
|
C | T | 3 | a0001c0001t0004g0289a0001c0001t0004g0299a0001c0001t0032g0296 | 3 | NA18939.hp1 NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1637+2403C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485023 | ||||||
chr6:73485046
|
C | CA | 60 | a0001c0001t0007g0312a0001c0001t0008g0120a0001c0001t0016g0093others(57): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1637+2443dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485046 | |||||
chr6:73485046
|
CA | C | 9 | a0001c0001t0001g0182a0001c0001t0001g0245a0001c0001t0010g0301others(6): Show | 9 | HG01109.hp2 HG02818.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637+2443delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485046 | |||||
chr6:73485106
|
A | G | 1 | a0001c0001t0005g0359 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1637+2486A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485106 | ||||||
chr6:73485205
|
A | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+2585A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485205 | ||||||
chr6:73485229
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1637+2609A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485229 | ||||||
chr6:73485436
|
T | C | 3 | a0001c0001t0007g0233a0001c0001t0036g0164a0001c0001t0036g0174 | 3 | HG02071.hp1 NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1637+2816T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485436 | ||||||
chr6:73485441
|
C | CT | 15 | a0001c0001t0001g0316a0001c0001t0005g0349a0001c0001t0005g0364others(12): Show | 15 | HG01109.hp1 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1637+2836dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | |||||
chr6:73485441
|
C | CTTT | 10 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(7): Show | 10 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1637+2834_1637+283 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | |||||
chr6:73485441
|
CT | C | 6 | a0001c0001t0001g0133a0001c0001t0008g0346a0001c0001t0061g0300others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+2836delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485441 | |||||
chr6:73485481
|
T | C | 379 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(376): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1637+2861T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485481 | ||||||
chr6:73485583
|
C | T | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1637+2963C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485583 | ||||||
chr6:73485589
|
C | G | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+2969C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485589 | ||||||
chr6:73485611
|
G | A | 1 | a0001c0001t0007g0312 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1637+2991G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485611 | ||||||
chr6:73485736
|
T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1637+3116T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485736 | ||||||
chr6:73485808
|
C | T | 340 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(337): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1637+3188C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485808 | ||||||
chr6:73485925
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+3305C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485925 | ||||||
chr6:73485932
|
G | A | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+3312G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485932 | ||||||
chr6:73485940
|
TACAC | T | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1637+3336_1637+333 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73485940 | |||||
chr6:73485961
|
T | C | 2 | a0001c0002t0021g0071a0001c0002t0021g0080 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1637+3341T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73485961 | ||||||
chr6:73486040
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1637+3420A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486040 | ||||||
chr6:73486113
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1637+3493A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486113 | ||||||
chr6:73486182
|
A | C | 1 | a0001c0001t0035g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1637+3562A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486182 | ||||||
chr6:73486258
|
A | T | 258 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(255): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1637+3638A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486258 | ||||||
chr6:73486341
|
A | G | 1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1637+3721A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486341 | ||||||
chr6:73486425
|
CTATGGAT others(8): Show |
C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1637+3806_1637+382 others(19): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486425 | ||||||
chr6:73486429
|
G | A | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1637+3809G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486429 | ||||||
chr6:73486430
|
G | T | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1637+3810G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486430 | ||||||
chr6:73486487
|
C | G | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+3867C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486487 | ||||||
chr6:73486496
|
A | G | 343 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(340): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1637+3876A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486496 | ||||||
chr6:73486567
|
G | A | 15 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0214others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1637+3947G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486567 | ||||||
chr6:73486641
|
G | A | 1 | a0001c0001t0009g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1637+4021G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486641 | ||||||
chr6:73486766
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4146G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486766 | ||||||
chr6:73486784
|
T | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4164T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486784 | ||||||
chr6:73486880
|
C | G | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1637+4260C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73486880 | ||||||
chr6:73487011
|
G | GGAT | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1637+4392_1637+439 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487011 | |||||
chr6:73487096
|
C | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1637+4476C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487096 | ||||||
chr6:73487151
|
G | A | 1 | a0001c0002t0002g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1637+4531G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487151 | ||||||
chr6:73487197
|
AT | A | 285 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(282): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1637+4597delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | |||||
chr6:73487197
|
ATT | A | 21 | a0001c0001t0001g0324a0001c0001t0004g0276a0001c0001t0006g0251others(18): Show | 21 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1637+4596_1637+459 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | |||||
chr6:73487197
|
ATTT | A | 53 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(50): Show | 53 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1637+4595_1637+459 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487197 | |||||
chr6:73487249
|
G | C | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1637+4629G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487249 | ||||||
chr6:73487556
|
G | GT | 40 | a0001c0001t0001g0308a0001c0001t0005g0018a0001c0001t0005g0020others(37): Show | 43 | HG00438.hp2 HG00642.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1638-4662dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487556 | |||||
chr6:73487556
|
GT | G | 55 | a0001c0001t0001g0178a0001c0001t0003g0001a0001c0001t0003g0002others(52): Show | 60 | HG00544.hp2 HG00735.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.1638-4662delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487556 | |||||
chr6:73487577
|
G | GT | 34 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(31): Show | 39 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1638-4645dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73487577 | |||||
chr6:73487604
|
G | A | 1 | a0001c0001t0012g0220 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1638-4630G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487604 | ||||||
chr6:73487792
|
C | T | 1 | a0001c0002t0011g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1638-4442C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487792 | ||||||
chr6:73487809
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-4425G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487809 | ||||||
chr6:73487825
|
C | T | 55 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1638-4409C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487825 | ||||||
chr6:73487938
|
G | A | 79 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1638-4296G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487938 | ||||||
chr6:73487947
|
A | G | 2 | a0001c0001t0073g0161a0001c0001t0094g0166 | 2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1638-4287A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73487947 | ||||||
chr6:73488232
|
G | T | 19 | a0001c0001t0001g0136a0001c0001t0001g0178a0001c0001t0001g0182others(16): Show | 20 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1638-4002G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488232 | ||||||
chr6:73488452
|
C | T | 1 | a0001c0002t0002g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1638-3782C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488452 | ||||||
chr6:73488554
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0199others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638-3680C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488554 | ||||||
chr6:73488572
|
T | C | 1 | a0001c0002t0020g0078 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1638-3662T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488572 | ||||||
chr6:73488618
|
A | T | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1638-3616A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488618 | ||||||
chr6:73488814
|
G | A | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1638-3420G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488814 | ||||||
chr6:73488956
|
C | T | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-3278C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73488956 | ||||||
chr6:73489077
|
C | A | 4 | a0001c0001t0017g0336a0001c0001t0017g0357a0001c0001t0017g0360others(1): Show | 4 | HG02970.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-3157C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489077 | ||||||
chr6:73489125
|
A | G | 5 | a0001c0002t0029g0008a0001c0002t0029g0083a0001c0002t0029g0084others(2): Show | 5 | HG02165.hp1 NA18969.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-3109A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489125 | ||||||
chr6:73489278
|
C | CT | 187 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(184): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1638-2944dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73489278 | |||||
chr6:73489278
|
CT | C | 13 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0021others(10): Show | 16 | HG01496.hp1 HG01978.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.1638-2944delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73489278 | |||||
chr6:73489285
|
T | C | 1 | a0001c0002t0011g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1638-2949T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489285 | ||||||
chr6:73489442
|
C | G | 1 | a0001c0001t0009g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1638-2792C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489442 | ||||||
chr6:73489619
|
C | A | 2 | a0001c0001t0010g0301a0001c0001t0010g0302 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1638-2615C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489619 | ||||||
chr6:73489720
|
A | G | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-2514A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489720 | ||||||
chr6:73489724
|
T | A | 6 | a0001c0001t0009g0126a0001c0001t0009g0127a0001c0001t0009g0128others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638-2510T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489724 | ||||||
chr6:73489760
|
C | A | 1 | a0001c0001t0006g0195 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1638-2474C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489760 | ||||||
chr6:73489795
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(198): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1638-2439G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73489795 | ||||||
chr6:73490051
|
A | G | 8 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638-2183A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490051 | ||||||
chr6:73490076
|
G | A | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1638-2158G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490076 | ||||||
chr6:73490376
|
C | T | 5 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0366others(2): Show | 5 | NA18946.hp2 NA18957.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1858C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490376 | ||||||
chr6:73490383
|
G | C | 57 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 57 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1638-1851G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490383 | ||||||
chr6:73490464
|
TG | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1638-1769delG | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490464 | ||||||
chr6:73490545
|
A | G | 1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1638-1689A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490545 | ||||||
chr6:73490680
|
C | T | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1638-1554C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490680 | ||||||
chr6:73490723
|
T | TA | 82 | a0001c0001t0001g0268a0001c0001t0001g0306a0001c0001t0076g0270others(79): Show | 82 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1638-1500dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73490723 | |||||
chr6:73490752
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1638-1482C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490752 | ||||||
chr6:73490934
|
A | C | 10 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(7): Show | 10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-1300A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490934 | ||||||
chr6:73490940
|
A | G | 2 | a0001c0001t0024g0256a0001c0001t0024g0257 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1638-1294A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73490940 | ||||||
chr6:73491003
|
A | G | 151 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(148): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1638-1231A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491003 | ||||||
chr6:73491118
|
A | G | 1 | a0001c0002t0123g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1638-1116A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491118 | ||||||
chr6:73491122
|
A | C | 2 | a0001c0002t0002g0044a0001c0002t0002g0051 | 2 | NA18941.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1638-1112A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491122 | ||||||
chr6:73491246
|
T | G | 14 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(11): Show | 14 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638-988T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491246 | ||||||
chr6:73491266
|
GA | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(333): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1638-954delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73491266 | |||||
chr6:73491307
|
G | A | 2 | a0001c0001t0031g0347a0001c0001t0031g0351 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1638-927G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491307 | ||||||
chr6:73491357
|
C | T | 2 | a0001c0001t0004g0015a0001c0001t0057g0294 | 3 | NA18962.hp2 NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1638-877C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491357 | ||||||
chr6:73491361
|
G | C | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(30): Show | 38 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1638-873G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491361 | ||||||
chr6:73491396
|
C | CA | 70 | a0001c0001t0003g0109a0001c0001t0004g0014a0001c0001t0004g0015others(67): Show | 72 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1638-821dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73491396 | |||||
chr6:73491408
|
A | G | 1 | a0001c0003t0030g0354 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1638-826A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491408 | ||||||
chr6:73491411
|
A | AG | 11 | a0001c0001t0001g0158a0001c0001t0001g0310a0001c0001t0007g0145others(8): Show | 11 | HG00597.hp1 HG02074.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1638-823_1638-822i others(3): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491411 | ||||||
chr6:73491411
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(140): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1638-823A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491411 | ||||||
chr6:73491558
|
G | A | 1 | a0001c0002t0029g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1638-676G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491558 | ||||||
chr6:73491703
|
A | G | 1 | a0001c0002t0114g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1638-531A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491703 | ||||||
chr6:73491878
|
A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1638-356A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491878 | ||||||
chr6:73491915
|
G | A | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1638-319G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491915 | ||||||
chr6:73491947
|
A | C | 1 | a0001c0001t0045g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1638-287A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491947 | ||||||
chr6:73491953
|
A | T | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1638-281A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73491953 | ||||||
chr6:73492010
|
G | A | 1 | a0001c0002t0002g0026 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1638-224G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492010 | ||||||
chr6:73492090
|
C | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(183): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1638-144C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492090 | ||||||
chr6:73492103
|
CA | C | 236 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0001g0131others(233): Show | 243 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1638-116delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73492103 | |||||
chr6:73492103
|
CAA | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0158others(103): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1638-117_1638-116d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr6 | 73492103 | |||||
chr6:73492169
|
C | T | 1 | a0001c0001t0009g0238 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1638-65C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492169 | ||||||
chr6:73492194
|
C | T | 2 | a0001c0001t0015g0205a0001c0001t0015g0287 | 2 | NA18944.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1638-40C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 9/11 | chr6 | 73492194 | ||||||
chr6:73492437
|
A | C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+85A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492437 | ||||||
chr6:73492550
|
T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1756+198T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492550 | ||||||
chr6:73492604
|
A | G | 1 | a0001c0001t0014g0286 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1756+252A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492604 | ||||||
chr6:73492655
|
T | C | 2 | a0001c0001t0040g0193a0001c0001t0040g0260 | 2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1756+303T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492655 | ||||||
chr6:73492676
|
G | A | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1756+324G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492676 | ||||||
chr6:73492708
|
G | C | 2 | a0001c0002t0002g0036a0001c0002t0002g0039 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1756+356G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492708 | ||||||
chr6:73492756
|
T | C | 2 | a0001c0001t0036g0164a0001c0001t0036g0174 | 2 | NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1756+404T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492756 | ||||||
chr6:73492801
|
A | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(184): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1756+449A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492801 | ||||||
chr6:73492806
|
T | TA | 208 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(205): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1756+470dupA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492806 | |||||
chr6:73492806
|
T | TAA | 132 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(129): Show | 134 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1756+469_1756+470d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492806 | |||||
chr6:73492968
|
A | ATGTG | 10 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(7): Show | 10 | HG01884.hp1 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+638_1756+641d others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTG | 55 | a0001c0001t0017g0361a0001c0001t0089g0248a0001c0002t0002g0007others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1756+636_1756+641d others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTGT others(1): Show |
68 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(65): Show | 70 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1756+634_1756+641d others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTGT others(3): Show |
28 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0021others(25): Show | 31 | HG00741.hp1 HG01074.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1756+632_1756+641d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTGT others(5): Show |
12 | a0001c0001t0008g0019a0001c0001t0008g0330a0001c0001t0008g0337others(9): Show | 12 | HG02055.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1756+630_1756+641d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTGT others(7): Show |
4 | a0001c0001t0005g0359a0001c0001t0008g0338a0001c0001t0017g0360others(1): Show | 4 | HG02965.hp1 HG03017.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+628_1756+641d others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0097g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1756+626_1756+641d others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492968 | |||||
chr6:73492968
|
A | G | 4 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092others(1): Show | 4 | HG01109.hp2 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+616A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492968 | ||||||
chr6:73492992
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0053g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1756+641_1756+642i others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73492992 | |||||
chr6:73492993
|
T | TGTGTGTG others(4): Show |
4 | a0001c0001t0016g0185a0001c0001t0025g0140a0001c0001t0025g0141others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+641_1756+642i others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492993 | ||||||
chr6:73492993
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0016g0366 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1756+641_1756+642i others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492993 | ||||||
chr6:73492994
|
A | G | 190 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(187): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1756+642A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492994 | ||||||
chr6:73492994
|
A | T | 12 | a0001c0001t0004g0276a0001c0001t0004g0280a0001c0001t0016g0185others(9): Show | 12 | HG01106.hp2 HG01255.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1756+642A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492994 | ||||||
chr6:73492995
|
T | TGTA | 3 | a0001c0001t0007g0233a0001c0001t0036g0164a0001c0001t0036g0174 | 3 | HG02071.hp1 NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1756+643_1756+644i others(5): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492995
|
T | TGTGTA | 20 | a0001c0001t0001g0182a0001c0001t0003g0001a0001c0001t0003g0098others(17): Show | 23 | HG02004.hp2 HG03491.hp2 HG03492.hp2 others(20): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492995
|
T | TGTGTGTA | 142 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0134others(139): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(9): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492995
|
T | TGTGTGTG others(2): Show |
20 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0001g0131others(17): Show | 21 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1756+643_1756+644i others(11): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492995
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1756+643_1756+644i others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492995
|
T | TGTGTGTG others(14): Show |
3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1756+643_1756+644i others(23): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492995 | ||||||
chr6:73492996
|
T | A | 1 | a0001c0001t0089g0248 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1756+644T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73492996 | ||||||
chr6:73493035
|
C | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(184): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1756+683C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493035 | ||||||
chr6:73493087
|
C | T | 11 | a0001c0002t0021g0071a0001c0002t0021g0080a0001c0002t0021g0087others(8): Show | 11 | HG01884.hp1 HG02165.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1756+735C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493087 | ||||||
chr6:73493206
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1756+854G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493206 | ||||||
chr6:73493350
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1756+998A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493350 | ||||||
chr6:73493354
|
A | ATG | 138 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0009others(135): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1756+1036_1756+103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTG | 27 | a0001c0001t0003g0106a0001c0001t0003g0114a0001c0001t0004g0277others(24): Show | 27 | HG00621.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1756+1034_1756+103 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTGTG | 17 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 18 | HG01884.hp2 HG02015.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1756+1032_1756+103 others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTGTGT others(1): Show |
31 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0158others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1756+1030_1756+103 others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTGTGT others(3): Show |
17 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0230others(14): Show | 19 | HG00438.hp1 HG00621.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1756+1028_1756+103 others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTGTGT others(5): Show |
40 | a0001c0001t0001g0134a0001c0001t0001g0170a0001c0001t0001g0218others(37): Show | 41 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1756+1026_1756+103 others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | ATGTGTGT others(7): Show |
11 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0242others(8): Show | 11 | HG01516.hp1 HG01517.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.1756+1024_1756+103 others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1756+1002A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493354 | ||||||
chr6:73493354
|
ATG | A | 42 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0021others(39): Show | 45 | HG00741.hp1 HG01074.hp2 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.1756+1036_1756+103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
ATGTG | A | 22 | a0001c0001t0016g0185a0001c0001t0016g0186a0001c0001t0025g0140others(19): Show | 22 | HG02165.hp1 HG02257.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.1756+1034_1756+103 others(8): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
ATGTGTG | A | 10 | a0001c0001t0016g0094a0001c0002t0021g0071a0001c0002t0021g0080others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1756+1032_1756+103 others(10): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493354
|
ATGTGTGT others(7): Show |
A | 4 | a0001c0001t0015g0205a0001c0001t0015g0287a0001c0001t0015g0297others(1): Show | 4 | NA18944.hp1 NA18973.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+1024_1756+103 others(18): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73493354 | |||||
chr6:73493389
|
T | TGTGTGTG others(2): Show |
3 | a0001c0001t0009g0309a0001c0001t0083g0262a0001c0001t0085g0171 | 3 | HG01192.hp1 NA18978.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1756+1037_1756+103 others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | ||||||
chr6:73493389
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0084g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1756+1037_1756+103 others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | ||||||
chr6:73493389
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1756+1037_1756+103 others(17): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493389 | ||||||
chr6:73493391
|
T | G | 1 | a0001c0001t0083g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1756+1039T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493391 | ||||||
chr6:73493638
|
G | A | 1 | a0001c0001t0019g0100 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1756+1286G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493638 | ||||||
chr6:73493641
|
T | C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1289T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493641 | ||||||
chr6:73493702
|
A | G | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1350A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493702 | ||||||
chr6:73493824
|
C | T | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1756+1472C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493824 | ||||||
chr6:73493896
|
G | A | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1756+1544G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73493896 | ||||||
chr6:73494012
|
C | G | 1 | a0001c0002t0002g0038 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1756+1660C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494012 | ||||||
chr6:73494109
|
C | T | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1756+1757C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494109 | ||||||
chr6:73494163
|
A | G | 1 | a0001c0001t0014g0293 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1756+1811A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494163 | ||||||
chr6:73494436
|
A | T | 1 | a0001c0001t0016g0093 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1756+2084A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494436 | ||||||
chr6:73494479
|
C | CT | 15 | a0001c0001t0012g0123a0001c0001t0016g0093a0001c0001t0016g0094others(12): Show | 15 | HG01175.hp1 HG02622.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.1756+2142dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494479 | |||||
chr6:73494479
|
CT | C | 76 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(73): Show | 76 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1756+2142delT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494479 | |||||
chr6:73494508
|
G | A | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1756+2156G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494508 | ||||||
chr6:73494516
|
G | C | 2 | a0001c0002t0011g0054a0001c0002t0038g0032 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1756+2164G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494516 | ||||||
chr6:73494528
|
T | C | 2 | a0001c0001t0024g0256a0001c0001t0024g0257 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1756+2176T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494528 | ||||||
chr6:73494538
|
G | A | 1 | a0001c0001t0010g0016 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1756+2186G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494538 | ||||||
chr6:73494658
|
G | A | 7 | a0001c0001t0016g0093a0001c0001t0016g0094a0001c0001t0016g0185others(4): Show | 7 | HG03209.hp2 NA18946.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1756+2306G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494658 | ||||||
chr6:73494723
|
G | A | 10 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(7): Show | 10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+2371G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494723 | ||||||
chr6:73494775
|
C | CT | 79 | a0001c0001t0001g0218a0001c0001t0001g0310a0001c0001t0019g0100others(76): Show | 79 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1756+2437dupT | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73494775 | |||||
chr6:73494778
|
T | C | 1 | a0001c0001t0014g0327 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1756+2426T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494778 | ||||||
chr6:73494928
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1756+2576C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73494928 | ||||||
chr6:73495084
|
A | G | 1 | a0001c0001t0046g0329 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1757-2652A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495084 | ||||||
chr6:73495319
|
G | A | 1 | a0001c0001t0005g0348 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1757-2417G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495319 | ||||||
chr6:73495402
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1757-2334C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495402 | ||||||
chr6:73495597
|
C | T | 5 | a0001c0002t0029g0008a0001c0002t0029g0083a0001c0002t0029g0084others(2): Show | 5 | HG02165.hp1 NA18969.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-2139C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495597 | ||||||
chr6:73495908
|
G | A | 342 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(339): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1757-1828G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73495908 | ||||||
chr6:73496035
|
A | G | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1757-1701A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496035 | ||||||
chr6:73496038
|
A | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1757-1698A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496038 | ||||||
chr6:73496129
|
G | A | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1757-1607G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496129 | ||||||
chr6:73496233
|
G | A | 1 | a0001c0001t0034g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1757-1503G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496233 | ||||||
chr6:73496285
|
C | T | 2 | a0001c0002t0121g0081a0001c0002t0122g0085 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1757-1451C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496285 | ||||||
chr6:73496320
|
T | C | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1416T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496320 | ||||||
chr6:73496440
|
T | A | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1296T>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496440 | ||||||
chr6:73496441
|
A | T | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1295A>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496441 | ||||||
chr6:73496442
|
T | C | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1757-1294T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496442 | ||||||
chr6:73496625
|
A | AC | 11 | a0001c0001t0003g0111a0001c0001t0005g0362a0001c0001t0006g0187others(8): Show | 11 | HG01175.hp1 HG01496.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1757-1106dupC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73496625 | |||||
chr6:73496625
|
A | C | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1757-1111A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496625 | ||||||
chr6:73496631
|
T | C | 4 | a0001c0001t0012g0244a0001c0001t0032g0322a0001c0001t0048g0339others(1): Show | 4 | HG01978.hp2 HG02055.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757-1105T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496631 | ||||||
chr6:73496631
|
T | TC | 7 | a0001c0001t0025g0142a0001c0001t0034g0138a0001c0001t0058g0288others(4): Show | 7 | HG01358.hp2 HG01928.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1757-1099dupC | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73496631 | |||||
chr6:73496632
|
C | T | 1 | a0004c0005t0026g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1757-1104C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496632 | ||||||
chr6:73496776
|
C | T | 3 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0004g0281 | 3 | HG00639.hp2 HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1757-960C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496776 | ||||||
chr6:73496778
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1757-958G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496778 | ||||||
chr6:73496781
|
A | G | 1 | a0001c0001t0042g0363 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1757-955A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496781 | ||||||
chr6:73496886
|
C | A | 1 | a0001c0002t0029g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1757-850C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496886 | ||||||
chr6:73496913
|
C | T | 4 | a0001c0001t0017g0336a0001c0001t0017g0357a0001c0001t0017g0360others(1): Show | 4 | HG02970.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1757-823C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496913 | ||||||
chr6:73496914
|
G | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0009g0304others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757-822G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496914 | ||||||
chr6:73496968
|
T | C | 13 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0021others(10): Show | 16 | HG01496.hp1 HG01978.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.1757-768T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73496968 | ||||||
chr6:73497002
|
C | T | 3 | a0001c0001t0034g0138a0001c0001t0034g0149a0001c0001t0065g0152 | 3 | HG00280.hp1 HG01358.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1757-734C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497002 | ||||||
chr6:73497084
|
CAT | C | 3 | a0001c0001t0097g0143a0001c0001t0099g0137a0001c0001t0100g0153 | 3 | HG02717.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1757-650_1757-649d others(4): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497084 | |||||
chr6:73497157
|
C | CTTTTTTT others(3): Show |
39 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0001g0245others(36): Show | 44 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1757-575_1757-566d others(12): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | |||||
chr6:73497157
|
C | CTTTTTTT others(4): Show |
205 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0130others(202): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1757-576_1757-566d others(13): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | |||||
chr6:73497157
|
C | CTTTTTTT others(5): Show |
69 | a0001c0001t0001g0131a0001c0001t0001g0178a0001c0001t0001g0246others(66): Show | 69 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1757-577_1757-566d others(14): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | |||||
chr6:73497157
|
C | CTTTTTTT others(6): Show |
21 | a0001c0001t0004g0292a0001c0001t0016g0185a0001c0002t0002g0025others(18): Show | 21 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1757-578_1757-566d others(15): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | |||||
chr6:73497157
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0011g0068a0001c0002t0127g0082 | 2 | HG02738.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1757-566_1757-565i others(16): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 73497157 | |||||
chr6:73497240
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1757-496C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497240 | ||||||
chr6:73497373
|
C | T | 1 | a0001c0001t0025g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1757-363C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497373 | ||||||
chr6:73497399
|
C | T | 3 | a0001c0001t0006g0195a0001c0001t0006g0254a0001c0001t0081g0253 | 3 | NA18982.hp2 NA19002.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1757-337C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497399 | ||||||
chr6:73497468
|
T | C | 1 | a0001c0001t0008g0337 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1757-268T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 10/11 | chr6 | 73497468 | ||||||
chr6:73498107
|
G | C | 2 | a0001c0001t0005g0358a0001c0001t0005g0359 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1917+211G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498107 | ||||||
chr6:73498222
|
A | G | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1917+326A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498222 | ||||||
chr6:73498315
|
G | A | 1 | a0001c0002t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1917+419G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498315 | ||||||
chr6:73498333
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1917+437T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498333 | ||||||
chr6:73498349
|
C | G | 1 | a0001c0001t0045g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1917+453C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498349 | ||||||
chr6:73498448
|
T | C | 78 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(75): Show | 78 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1917+552T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498448 | ||||||
chr6:73498572
|
G | C | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1917+676G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498572 | ||||||
chr6:73498744
|
G | T | 2 | a0001c0001t0006g0194a0001c0001t0024g0263 | 2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1917+848G>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498744 | ||||||
chr6:73498793
|
C | T | 63 | a0001c0001t0057g0294a0001c0002t0002g0007a0001c0002t0002g0025others(60): Show | 63 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1917+897C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498793 | ||||||
chr6:73498873
|
T | C | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1917+977T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498873 | ||||||
chr6:73498919
|
G | A | 1 | a0001c0001t0105g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1917+1023G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73498919 | ||||||
chr6:73499006
|
C | T | 3 | a0001c0002t0027g0090a0001c0002t0027g0091a0001c0002t0027g0092 | 3 | HG01109.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1917+1110C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499006 | ||||||
chr6:73499007
|
G | A | 1 | a0001c0002t0111g0062 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1917+1111G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499007 | ||||||
chr6:73499066
|
C | G | 5 | a0001c0001t0007g0303a0001c0001t0007g0325a0001c0001t0060g0173others(2): Show | 5 | NA18969.hp1 NA19056.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.1917+1170C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499066 | ||||||
chr6:73499090
|
A | C | 1 | a0001c0001t0016g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1917+1194A>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499090 | ||||||
chr6:73499276
|
G | C | 1 | a0001c0001t0007g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1918-1298G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499276 | ||||||
chr6:73499437
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1918-1137G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499437 | ||||||
chr6:73499521
|
C | CAA | 65 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(62): Show | 65 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1918-1040_1918-103 others(6): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | |||||
chr6:73499521
|
C | CAAA | 12 | a0001c0002t0002g0038a0001c0002t0011g0068a0001c0002t0020g0072others(9): Show | 12 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1918-1041_1918-103 others(7): Show |
MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | |||||
chr6:73499521
|
CA | C | 15 | a0001c0001t0001g0133a0001c0001t0008g0121a0001c0001t0016g0093others(12): Show | 15 | HG02622.hp2 HG02717.hp2 HG02897.hp1 others(12): Show |
intron_variant | MODIFIER | c.1918-1039delA | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 73499521 | |||||
chr6:73499536
|
G | A | 1 | a0001c0002t0115g0024 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1918-1038G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499536 | ||||||
chr6:73499586
|
C | A | 2 | a0001c0002t0021g0071a0001c0002t0021g0080 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1918-988C>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499586 | ||||||
chr6:73499620
|
G | A | 1 | a0001c0001t0070g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1918-954G>A | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499620 | ||||||
chr6:73499740
|
T | C | 81 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0026others(78): Show | 81 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1918-834T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499740 | ||||||
chr6:73499827
|
T | C | 1 | a0002c0009t0010g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1918-747T>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499827 | ||||||
chr6:73499946
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0035g0135 | 3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1918-628C>T | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499946 | ||||||
chr6:73499992
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0035g0135 | 3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1918-582A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73499992 | ||||||
chr6:73500044
|
G | C | 1 | a0001c0001t0007g0212 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1918-530G>C | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500044 | ||||||
chr6:73500090
|
C | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1918-484C>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500090 | ||||||
chr6:73500202
|
A | G | 1 | a0001c0001t0082g0259 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1918-372A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500202 | ||||||
chr6:73500240
|
A | G | 1 | a0001c0001t0067g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1918-334A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500240 | ||||||
chr6:73500346
|
A | G | 57 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0132others(54): Show | 59 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1918-228A>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500346 | ||||||
chr6:73500567
|
T | G | 10 | a0001c0002t0020g0072a0001c0002t0020g0075a0001c0002t0020g0076others(7): Show | 10 | HG02257.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1918-7T>G | MTO1 | ENSG00000135297.17 | transcript | ENST00000498286.6 | protein_coding | 11/11 | chr6 | 73500567 |