geneid | 167838 |
---|---|
ensemblid | ENSG00000164440.15 |
hgncid | 21617 |
symbol | TXLNB |
name | taxilin beta |
refseq_nuc | NM_153235.4 |
refseq_prot | NP_694967.3 |
ensembl_nuc | ENST00000358430.8 |
ensembl_prot | ENSP00000351206.3 |
mane_status | MANE Select |
chr | chr6 |
start | 139240061 |
end | 139291998 |
strand | - |
ver | v1.2 |
region | chr6:139240061-139291998 |
region5000 | chr6:139235061-139296998 |
regionname0 | TXLNB_chr6_139240061_139291998 |
regionname5000 | TXLNB_chr6_139235061_139296998 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 684 | 115 | 10 | 21 | 61 | 6 | 16 | 44 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002 | 0/1 | 684 | 98 | 25 | 21 | 34 | 2 | 15 | 26 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003 | 0/0 | 684 | 38 | 25 | 8 | 0 | 2 | 3 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004 | 0/0 | 684 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005 | 0/0 | 684 | 8 | 5 | 0 | 3 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006 | 0/0 | 684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0007 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0008 | 0/0 | 684 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0009 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0010 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0011 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0012 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0013 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0014 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0015 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0016 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0017 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0018 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2055 | 102 | 10 | 21 | 48 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0002 | 0/1 | 2055 | 88 | 19 | 21 | 31 | 2 | 14 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0003 | 0/0 | 2055 | 20 | 10 | 7 | 0 | 1 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0004 | 0/0 | 2055 | 12 | 0 | 0 | 12 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0005 | 0/0 | 2055 | 7 | 5 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0006 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0007 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0008 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0009 | 0/0 | 2055 | 6 | 5 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0010 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0011 | 0/0 | 2055 | 4 | 2 | 0 | 0 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0012 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0013 | 0/0 | 2055 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0014 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0015 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0016 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0017 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0018 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0019 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0020 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0021 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0022 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0023 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0024 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0025 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0026 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0027 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0028 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0029 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0030 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0031 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0032 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0033 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
c0034 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2558 | 120 | 12 | 21 | 64 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0002 | 0/0 | 2555 | 44 | 28 | 7 | 7 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0003 | 0/1 | 2555 | 41 | 8 | 12 | 11 | 0 | 9 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0004 | 0/0 | 2558 | 18 | 9 | 7 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0005 | 0/0 | 2555 | 17 | 16 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0006 | 0/0 | 2555 | 9 | 0 | 0 | 8 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0007 | 0/0 | 2555 | 6 | 0 | 2 | 0 | 1 | 3 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0008 | 0/0 | 2549 | 5 | 5 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0009 | 0/0 | 2555 | 3 | 1 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0010 | 0/0 | 2558 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0011 | 0/0 | 2555 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0012 | 0/0 | 2555 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0013 | 0/0 | 2555 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0014 | 0/0 | 2555 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0015 | 0/0 | 2558 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0016 | 0/0 | 2558 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0017 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0018 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0019 | 0/0 | 2555 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0020 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0021 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0022 | 0/0 | 2555 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0023 | 0/0 | 2555 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0024 | 0/0 | 2555 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0025 | 0/0 | 2555 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0026 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0027 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0028 | 0/0 | 2555 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0029 | 0/0 | 2558 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0030 | 0/0 | 2558 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0031 | 0/0 | 2558 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
t0032 | 0/0 | 2555 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 6 | 0 | 2 | 2 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2055 | 102 | 10 | 21 | 48 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0004 | 0/0 | 2055 | 12 | 0 | 0 | 12 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0028 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002 | 0/1 | 2055 | 88 | 19 | 21 | 31 | 2 | 14 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0009 | 0/0 | 2055 | 6 | 5 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0016 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0025 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0030 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0003 | 0/0 | 2055 | 20 | 10 | 7 | 0 | 1 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0008 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0011 | 0/0 | 2055 | 4 | 2 | 0 | 0 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0012 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0014 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0031 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0005 | 0/0 | 2055 | 7 | 5 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0006 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0017 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0010 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0013 | 0/0 | 2055 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006c0007 | 0/0 | 2055 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006c0018 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0007c0023 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0007c0034 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0008c0015 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0009c0032 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0010c0021 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0011c0022 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0012c0033 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0013c0026 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0014c0027 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0015c0024 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0016c0029 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0017c0020 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0018c0019 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4612 | 96 | 10 | 20 | 43 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0001t0003 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0001t0015 | 0/0 | 4612 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0001t0024 | 0/0 | 4609 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0001t0029 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0001t0030 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0004t0001 | 0/0 | 4612 | 12 | 0 | 0 | 12 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0001c0028t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0001 | 0/0 | 4612 | 6 | 0 | 0 | 6 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0002 | 0/0 | 4609 | 25 | 11 | 5 | 7 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0003 | 0/1 | 4609 | 37 | 7 | 11 | 10 | 0 | 8 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0006 | 0/0 | 4609 | 7 | 0 | 0 | 6 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0007 | 0/0 | 4609 | 6 | 0 | 2 | 0 | 1 | 3 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0009 | 0/0 | 4609 | 3 | 1 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0012 | 0/0 | 4609 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0023 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0002t0032 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0009t0002 | 0/0 | 4609 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0009t0003 | 0/0 | 4609 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0009t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0016t0006 | 0/0 | 4609 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0025t0003 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0002c0030t0003 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0003t0004 | 0/0 | 4612 | 18 | 9 | 7 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0003t0016 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0003t0031 | 0/0 | 4612 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0008t0001 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0008t0002 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0008t0008 | 0/0 | 4603 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0008t0026 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0011t0005 | 0/0 | 4609 | 2 | 1 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0011t0018 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0011t0019 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0012t0005 | 0/0 | 4609 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0012t0017 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0014t0008 | 0/0 | 4603 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0003c0031t0022 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0005t0002 | 0/0 | 4609 | 7 | 5 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0006t0005 | 0/0 | 4609 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0004c0017t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0010t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0010t0013 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0010t0014 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0005c0013t0010 | 0/0 | 4612 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006c0007t0002 | 0/0 | 4609 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006c0007t0005 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0006c0018t0016 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0007c0023t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0007c0034t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0008c0015t0011 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0009c0032t0028 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0010c0021t0001 | 0/0 | 4612 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0011c0022t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0012c0033t0020 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0013c0026t0025 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0014c0027t0021 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0015c0024t0027 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0016c0029t0002 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0017c0020t0002 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
a0018c0019t0001 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | copy fasta | chr6 | 139235061 | 139296998 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0024g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0029g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0030g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0028t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0001 | 0/1 | 6 | 0 | 2 | 2 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0012g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0023g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0032g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0016t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0016t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0025t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0030t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0016g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0031g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0019g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0031t0022g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0017t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0014g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0018t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0007c0023t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0007c0034t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0008c0015t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0008c0015t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0009c0032t0028g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0010c0021t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0011c0022t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0012c0033t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0013c0026t0025g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0014c0027t0021g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0015c0024t0027g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0016c0029t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0017c0020t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0018c0019t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00323 | hp2 | a0003 | c0003 | t0031 | g0236 | EUR | FIN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00438 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00558 | hp1 | a0002 | c0016 | t0006 | g0151 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0067 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0229 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0268 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0023 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00733 | hp2 | a0002 | c0002 | t0007 | g0230 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0186 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0239 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01069 | hp1 | a0003 | c0003 | t0004 | g0235 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0231 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01070 | hp2 | a0003 | c0003 | t0004 | g0187 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01071 | hp1 | a0003 | c0003 | t0004 | g0234 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01081 | hp1 | a0004 | c0005 | t0002 | g0143 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0079 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01099 | hp1 | a0002 | c0002 | t0023 | g0188 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01106 | hp2 | a0004 | c0005 | t0002 | g0144 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01109 | hp2 | a0003 | c0003 | t0004 | g0153 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01175 | hp1 | a0003 | c0003 | t0004 | g0237 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01243 | hp1 | a0003 | c0031 | t0022 | g0242 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01255 | hp1 | a0003 | c0003 | t0004 | g0080 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01255 | hp2 | a0002 | c0002 | t0009 | g0106 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01257 | hp2 | a0003 | c0003 | t0004 | g0238 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01261 | hp1 | a0010 | c0021 | t0001 | g0020 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01358 | hp1 | a0013 | c0026 | t0025 | g0211 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01358 | hp2 | a0002 | c0002 | t0007 | g0062 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0184 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0223 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0185 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01516 | hp1 | a0002 | c0002 | t0007 | g0097 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01884 | hp1 | a0012 | c0033 | t0020 | g0162 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01891 | hp1 | a0014 | c0027 | t0021 | g0244 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01891 | hp2 | a0003 | c0008 | t0008 | g0111 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01981 | hp1 | a0002 | c0002 | t0009 | g0049 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0183 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02015 | hp1 | a0001 | c0001 | t0029 | g0061 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02040 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02055 | hp1 | a0008 | c0015 | t0011 | g0255 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02055 | hp2 | a0003 | c0012 | t0005 | g0168 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02071 | hp1 | a0002 | c0016 | t0006 | g0150 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02071 | hp2 | a0001 | c0028 | t0001 | g0015 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02074 | hp1 | a0001 | c0001 | t0030 | g0042 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02074 | hp2 | a0001 | c0001 | t0015 | g0040 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02135 | hp1 | a0005 | c0013 | t0010 | g0158 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02145 | hp2 | a0005 | c0010 | t0013 | g0155 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0159 | EAS | CDX | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02257 | hp1 | a0003 | c0012 | t0017 | g0169 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02258 | hp1 | a0003 | c0008 | t0026 | g0110 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02258 | hp2 | a0004 | c0006 | t0005 | g0263 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0228 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0247 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0219 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02523 | hp1 | a0002 | c0002 | t0006 | g0087 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02572 | hp1 | a0004 | c0005 | t0002 | g0142 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02572 | hp2 | a0006 | c0007 | t0005 | g0180 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02615 | hp1 | a0004 | c0005 | t0002 | g0146 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0240 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02622 | hp1 | a0005 | c0010 | t0013 | g0154 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0198 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02630 | hp1 | a0002 | c0030 | t0003 | g0243 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02630 | hp2 | a0003 | c0011 | t0018 | g0152 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0218 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02683 | hp2 | a0002 | c0002 | t0007 | g0113 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0001 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02717 | hp1 | a0018 | c0019 | t0001 | g0253 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02717 | hp2 | a0004 | c0006 | t0005 | g0260 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0200 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02723 | hp2 | a0003 | c0011 | t0005 | g0121 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02809 | hp1 | a0011 | c0022 | t0005 | g0014 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02809 | hp2 | a0008 | c0015 | t0011 | g0254 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02886 | hp2 | a0003 | c0008 | t0002 | g0175 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02895 | hp1 | a0003 | c0014 | t0008 | g0165 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02897 | hp2 | a0003 | c0014 | t0008 | g0164 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02922 | hp1 | a0004 | c0005 | t0002 | g0145 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02922 | hp2 | a0002 | c0009 | t0005 | g0172 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02965 | hp1 | a0002 | c0009 | t0002 | g0166 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0246 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02970 | hp1 | a0002 | c0009 | t0002 | g0174 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02970 | hp2 | a0005 | c0010 | t0014 | g0157 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0182 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02976 | hp2 | a0003 | c0014 | t0008 | g0173 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03017 | hp1 | a0002 | c0002 | t0003 | g0213 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0195 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03098 | hp1 | a0003 | c0008 | t0002 | g0245 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03098 | hp2 | a0004 | c0006 | t0005 | g0259 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0249 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03139 | hp1 | a0006 | c0018 | t0016 | g0177 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03139 | hp2 | a0015 | c0024 | t0027 | g0130 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03195 | hp1 | a0003 | c0012 | t0005 | g0170 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03195 | hp2 | a0005 | c0010 | t0014 | g0156 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03209 | hp1 | a0003 | c0003 | t0004 | g0112 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03209 | hp2 | a0006 | c0007 | t0002 | g0179 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03225 | hp1 | a0005 | c0010 | t0005 | g0181 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03225 | hp2 | a0006 | c0007 | t0002 | g0261 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03453 | hp1 | a0003 | c0008 | t0008 | g0189 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03453 | hp2 | a0003 | c0003 | t0004 | g0196 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0224 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0148 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03491 | hp1 | a0002 | c0002 | t0007 | g0025 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03492 | hp1 | a0002 | c0002 | t0007 | g0024 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03516 | hp1 | a0006 | c0007 | t0005 | g0176 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03516 | hp2 | a0003 | c0008 | t0001 | g0192 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03579 | hp1 | a0006 | c0007 | t0002 | g0178 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03579 | hp2 | a0004 | c0006 | t0005 | g0256 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03669 | hp2 | a0003 | c0003 | t0004 | g0233 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03688 | hp1 | a0003 | c0011 | t0019 | g0116 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0208 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0214 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0069 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03831 | hp2 | a0003 | c0003 | t0004 | g0064 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0205 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04115 | hp2 | a0002 | c0025 | t0003 | g0251 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04199 | hp2 | a0002 | c0002 | t0032 | g0270 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0220 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0026 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18522 | hp2 | a0004 | c0017 | t0005 | g0257 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | CHB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18906 | hp1 | a0016 | c0029 | t0002 | g0201 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18944 | hp1 | a0002 | c0009 | t0003 | g0267 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18953 | hp1 | a0002 | c0002 | t0012 | g0215 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18956 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18960 | hp1 | a0002 | c0002 | t0006 | g0084 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18966 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18973 | hp1 | a0007 | c0023 | t0001 | g0068 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0264 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0139 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18978 | hp2 | a0002 | c0002 | t0006 | g0099 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18980 | hp2 | a0002 | c0002 | t0012 | g0209 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18983 | hp1 | a0002 | c0002 | t0006 | g0048 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18986 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18990 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18992 | hp2 | a0007 | c0034 | t0001 | g0265 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18995 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19001 | hp1 | a0001 | c0004 | t0001 | g0266 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19004 | hp2 | a0005 | c0013 | t0010 | g0119 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0197 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19030 | hp2 | a0002 | c0009 | t0002 | g0163 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0250 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19043 | hp2 | a0004 | c0005 | t0002 | g0147 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0269 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19068 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19087 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19090 | hp2 | a0005 | c0013 | t0010 | g0160 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19240 | hp1 | a0004 | c0005 | t0002 | g0141 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19240 | hp2 | a0003 | c0003 | t0004 | g0193 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0078 | AFR | ASW | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20129 | hp2 | a0004 | c0006 | t0005 | g0140 | AFR | ASW | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0212 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20805 | hp2 | a0003 | c0011 | t0005 | g0046 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02109 | hp1 | a0003 | c0003 | t0016 | g0149 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02109 | hp2 | a0017 | c0020 | t0002 | g0252 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02486 | hp1 | a0004 | c0006 | t0005 | g0258 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02559 | hp1 | a0006 | c0007 | t0002 | g0262 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02559 | hp2 | a0003 | c0012 | t0005 | g0171 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0199 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03471 | hp2 | a0009 | c0032 | t0028 | g0161 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG06807 | hp1 | a0002 | c0009 | t0002 | g0167 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG06807 | hp2 | a0003 | c0003 | t0004 | g0194 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20300 | hp2 | a0002 | c0002 | t0009 | g0070 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0001 | REF | REF | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0032 | REF | REF | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139242558
|
C | T | 1 | a0011 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2023G>A | p.Val675Met | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2115/4612 | 2023/2055 | 675/684 | chr6 | 139242558 | ||
chr6:139242747
|
C | T | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1834G>A | p.Gly612Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1926/4612 | 1834/2055 | 612/684 | chr6 | 139242747 | ||
chr6:139242777
|
C | G | 13 | a0002a0003a0004others(10): Show | 174 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(171): Show |
missense_variant | MODERATE | c.1804G>C | p.Ala602Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1896/4612 | 1804/2055 | 602/684 | chr6 | 139242777 | ||
chr6:139242800
|
G | A | 1 | a0013 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1781C>T | p.Pro594Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1873/4612 | 1781/2055 | 594/684 | chr6 | 139242800 | ||
chr6:139242980
|
G | C | 5 | a0005a0008a0009others(2): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
missense_variant | MODERATE | c.1601C>G | p.Ala534Gly | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1693/4612 | 1601/2055 | 534/684 | chr6 | 139242980 | ||
chr6:139243001
|
A | G | 1 | a0015 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1580T>C | p.Ile527Thr | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1672/4612 | 1580/2055 | 527/684 | chr6 | 139243001 | ||
chr6:139243041
|
C | T | 1 | a0007 | 2 | NA18973.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.1540G>A | p.Glu514Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1632/4612 | 1540/2055 | 514/684 | chr6 | 139243041 | ||
chr6:139255599
|
C | T | 9 | a0003a0004a0005others(6): Show | 67 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(64): Show |
missense_variant | MODERATE | c.1042G>A | p.Val348Met | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/10 | 1134/4612 | 1042/2055 | 348/684 | chr6 | 139255599 | ||
chr6:139260394
|
A | G | 1 | a0016 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.926T>C | p.Leu309Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1018/4612 | 926/2055 | 309/684 | chr6 | 139260394 | ||
chr6:139288550
|
C | T | 1 | a0010 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.350G>A | p.Gly117Glu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 442/4612 | 350/2055 | 117/684 | chr6 | 139288550 | ||
chr6:139288563
|
G | C | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.337C>G | p.Pro113Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 429/4612 | 337/2055 | 113/684 | chr6 | 139288563 | ||
chr6:139288581
|
C | T | 1 | a0017 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.319G>A | p.Glu107Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 411/4612 | 319/2055 | 107/684 | chr6 | 139288581 | ||
chr6:139288869
|
C | T | 4 | a0004a0006a0008others(1): Show | 24 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(21): Show |
missense_variant | MODERATE | c.31G>A | p.Ala11Thr | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 123/4612 | 31/2055 | 11/684 | chr6 | 139288869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139242667
|
T | C | 1 | a0002c0025 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1914A>G | p.Glu638Glu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2006/4612 | 1914/2055 | 638/684 | chr6 | 139242667 | ||
chr6:139242748
|
G | A | 3 | a0005c0010a0008c0015a0009c0032 | 8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
synonymous_variant | LOW | c.1833C>T | p.Ser611Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1925/4612 | 1833/2055 | 611/684 | chr6 | 139242748 | ||
chr6:139242831
|
A | G | 6 | a0005c0010a0005c0013a0008c0015others(3): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.1750T>C | p.Leu584Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1842/4612 | 1750/2055 | 584/684 | chr6 | 139242831 | ||
chr6:139242835
|
G | C | 6 | a0005c0010a0005c0013a0008c0015others(3): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.1746C>G | p.Ala582Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1838/4612 | 1746/2055 | 582/684 | chr6 | 139242835 | ||
chr6:139242964
|
C | T | 2 | a0003c0003a0006c0018 | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
synonymous_variant | LOW | c.1617G>A | p.Lys539Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1709/4612 | 1617/2055 | 539/684 | chr6 | 139242964 | ||
chr6:139260324
|
C | T | 4 | a0003c0011a0003c0012a0004c0006others(1): Show | 15 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
synonymous_variant | LOW | c.996G>A | p.Lys332Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1088/4612 | 996/2055 | 332/684 | chr6 | 139260324 | ||
chr6:139260405
|
C | A | 2 | a0001c0028a0002c0016 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
synonymous_variant | LOW | c.915G>T | p.Leu305Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1007/4612 | 915/2055 | 305/684 | chr6 | 139260405 | ||
chr6:139262765
|
C | T | 1 | a0004c0017 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.696G>A | p.Ala232Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/10 | 788/4612 | 696/2055 | 232/684 | chr6 | 139262765 | ||
chr6:139270582
|
T | C | 6 | a0003c0008a0003c0014a0003c0031others(3): Show | 19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
synonymous_variant | LOW | c.561A>G | p.Gln187Gln | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/10 | 653/4612 | 561/2055 | 187/684 | chr6 | 139270582 | ||
chr6:139288561
|
G | A | 2 | a0002c0030a0003c0031 | 2 | HG01243.hp1 HG02630.hp1 |
synonymous_variant | LOW | c.339C>T | p.Pro113Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 431/4612 | 339/2055 | 113/684 | chr6 | 139288561 | ||
chr6:139288618
|
T | C | 6 | a0001c0004a0002c0009a0003c0012others(3): Show | 27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
synonymous_variant | LOW | c.282A>G | p.Ser94Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 374/4612 | 282/2055 | 94/684 | chr6 | 139288618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139240079
|
T | G | 2 | a0003c0031t0022a0009c0032t0028 | 2 | HG01243.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2447A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2447 | chr6 | 139240079 | |||||
chr6:139240097
|
ATTATAG | A | 2 | a0003c0008t0008a0003c0014t0008 | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423_*2428delCTAT others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2423 | chr6 | 139240097 | |||||
chr6:139240101
|
T | C | 2 | a0003c0003t0016a0006c0018t0016 | 2 | HG02109.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2425A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2425 | chr6 | 139240101 | |||||
chr6:139240148
|
G | A | 1 | a0003c0003t0031 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2378 | chr6 | 139240148 | |||||
chr6:139240150
|
T | C | 1 | a0003c0011t0019 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2376A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2376 | chr6 | 139240150 | |||||
chr6:139240226
|
T | C | 1 | a0002c0002t0009 | 3 | HG01255.hp2 HG01981.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2300A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2300 | chr6 | 139240226 | |||||
chr6:139240299
|
C | T | 3 | a0002c0002t0006a0002c0002t0012a0002c0016t0006 | 11 | HG00438.hp1 HG00558.hp1 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2227 | chr6 | 139240299 | |||||
chr6:139240312
|
T | C | 3 | a0005c0010t0014a0012c0033t0020a0015c0024t0027 | 4 | HG01884.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2214A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2214 | chr6 | 139240312 | |||||
chr6:139240381
|
G | A | 13 | a0001c0001t0029a0002c0002t0002a0002c0009t0002others(10): Show | 54 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2145C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2145 | chr6 | 139240381 | |||||
chr6:139240419
|
T | A | 1 | a0002c0002t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2107 | chr6 | 139240419 | |||||
chr6:139240467
|
G | C | 14 | a0001c0001t0015a0001c0001t0024a0002c0002t0002others(11): Show | 56 | HG00597.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2059C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2059 | chr6 | 139240467 | |||||
chr6:139240594
|
T | C | 1 | a0013c0026t0025 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1932A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1932 | chr6 | 139240594 | |||||
chr6:139240660
|
G | T | 1 | a0003c0011t0018 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1866 | chr6 | 139240660 | |||||
chr6:139241137
|
T | G | 2 | a0014c0027t0021a0015c0024t0027 | 2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1389A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1389 | chr6 | 139241137 | |||||
chr6:139241199
|
T | C | 2 | a0014c0027t0021a0015c0024t0027 | 2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1327 | chr6 | 139241199 | |||||
chr6:139241277
|
C | T | 1 | a0003c0012t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1249 | chr6 | 139241277 | |||||
chr6:139241303
|
G | C | 26 | a0001c0001t0003a0001c0001t0024a0002c0002t0002others(23): Show | 117 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1223C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1223 | chr6 | 139241303 | |||||
chr6:139241383
|
T | G | 4 | a0003c0008t0008a0003c0008t0026a0003c0014t0008others(1): Show | 7 | HG01891.hp2 HG02258.hp1 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1143A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1143 | chr6 | 139241383 | |||||
chr6:139241727
|
T | C | 4 | a0002c0002t0006a0002c0002t0009a0002c0016t0006others(1): Show | 15 | HG00438.hp1 HG00558.hp1 HG01255.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 799 | chr6 | 139241727 | |||||
chr6:139241774
|
T | C | 8 | a0002c0002t0006a0002c0002t0009a0002c0016t0006others(5): Show | 22 | HG00438.hp1 HG00558.hp1 HG01255.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*752A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 752 | chr6 | 139241774 | |||||
chr6:139241890
|
T | A | 1 | a0002c0002t0007 | 6 | HG00733.hp2 HG01358.hp2 HG01516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 636 | chr6 | 139241890 | |||||
chr6:139241923
|
T | C | 1 | a0001c0001t0030 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 603 | chr6 | 139241923 | |||||
chr6:139241992
|
C | T | 1 | a0008c0015t0011 | 2 | HG02055.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*534G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 534 | chr6 | 139241992 | |||||
chr6:139242037
|
G | A | 1 | a0005c0013t0010 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 489 | chr6 | 139242037 | |||||
chr6:139242050
|
TATA | T | 43 | a0001c0001t0003a0001c0001t0024a0002c0002t0002others(40): Show | 146 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*473_*475delTAT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 473 | chr6 | 139242050 | |||||
chr6:139242485
|
T | C | 4 | a0003c0003t0004a0003c0003t0016a0003c0003t0031others(1): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*41A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 41 | chr6 | 139242485 | |||||
chr6:139242518
|
G | A | 4 | a0003c0003t0004a0003c0003t0016a0003c0003t0031others(1): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 8 | chr6 | 139242518 | |||||
chr6:139291939
|
G | C | 1 | a0002c0002t0032 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/10 | 3040 | chr6 | 139291939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139243453
|
T | C | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1267-139A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243453 | ||||||
chr6:139243492
|
C | CT | 117 | a0001c0001t0001g0043a0001c0001t0001g0124a0001c0001t0024g0139others(114): Show | 127 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(124): Show |
intron_variant | MODIFIER | c.1267-179dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | ||||||
chr6:139243492
|
C | CTT | 8 | a0002c0002t0002g0184a0002c0009t0002g0167a0003c0008t0008g0111others(5): Show | 8 | HG01243.hp1 HG01433.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1267-180_1267-179d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | ||||||
chr6:139243492
|
CT | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0058others(3): Show | 6 | HG00323.hp1 HG01175.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-179delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | ||||||
chr6:139243668
|
G | A | 3 | a0006c0007t0005g0176a0006c0007t0005g0180a0012c0033t0020g0162 | 3 | HG01884.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1267-354C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243668 | ||||||
chr6:139243851
|
C | T | 126 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(123): Show | 136 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(133): Show |
intron_variant | MODIFIER | c.1267-537G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243851 | ||||||
chr6:139243886
|
C | T | 2 | a0005c0010t0014g0156a0005c0010t0014g0157 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1267-572G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243886 | ||||||
chr6:139243967
|
G | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1266+628C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243967 | ||||||
chr6:139243968
|
C | T | 1 | a0002c0002t0009g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1266+627G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243968 | ||||||
chr6:139243992
|
T | C | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1266+603A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243992 | ||||||
chr6:139243994
|
TC | T | 22 | a0002c0002t0001g0221a0003c0003t0004g0064a0003c0003t0004g0080others(19): Show | 22 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1266+600delG | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243994 | ||||||
chr6:139244001
|
C | A | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1266+594G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244001 | ||||||
chr6:139244002
|
T | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1266+593A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244002 | ||||||
chr6:139244143
|
A | T | 6 | a0003c0008t0002g0245a0004c0005t0002g0141a0004c0005t0002g0143others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+452T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244143 | ||||||
chr6:139244261
|
A | G | 1 | a0002c0002t0003g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1266+334T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244261 | ||||||
chr6:139244535
|
G | A | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1266+60C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244535 | ||||||
chr6:139244832
|
T | C | 3 | a0002c0016t0006g0150a0002c0016t0006g0151a0016c0029t0002g0201 | 3 | HG00558.hp1 HG02071.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1171-142A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244832 | ||||||
chr6:139244847
|
A | G | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-157T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244847 | ||||||
chr6:139244952
|
T | C | 1 | a0003c0008t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1171-262A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244952 | ||||||
chr6:139245238
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1171-548T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245238 | ||||||
chr6:139245313
|
C | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-623G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245313 | ||||||
chr6:139245338
|
C | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-648G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245338 | ||||||
chr6:139245665
|
A | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-975T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245665 | ||||||
chr6:139245725
|
C | T | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1171-1035G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245725 | ||||||
chr6:139245762
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1171-1072C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245762 | ||||||
chr6:139245778
|
T | C | 1 | a0002c0002t0002g0239 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1171-1088A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245778 | ||||||
chr6:139245793
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1171-1103T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245793 | ||||||
chr6:139245807
|
C | T | 1 | a0004c0017t0005g0257 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1117G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245807 | ||||||
chr6:139245859
|
AT | A | 24 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(21): Show | 24 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1171-1170delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245859 | ||||||
chr6:139245883
|
AGT | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1195_1171-119 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245883 | ||||||
chr6:139245917
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1171-1227A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245917 | ||||||
chr6:139245939
|
C | T | 1 | a0002c0002t0006g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1171-1249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245939 | ||||||
chr6:139246030
|
G | A | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1171-1340C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246030 | ||||||
chr6:139246084
|
AT | A | 150 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(147): Show | 160 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.1171-1395delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246084 | ||||||
chr6:139246128
|
T | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1438A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246128 | ||||||
chr6:139246230
|
A | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1540T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246230 | ||||||
chr6:139246271
|
C | A | 150 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(147): Show | 160 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.1170+1546G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246271 | ||||||
chr6:139246386
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1170+1431C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246386 | ||||||
chr6:139246390
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1170+1427A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246390 | ||||||
chr6:139246428
|
C | T | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+1389G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246428 | ||||||
chr6:139246512
|
C | T | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+1305G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246512 | ||||||
chr6:139246531
|
A | G | 151 | a0001c0001t0001g0133a0001c0001t0024g0139a0002c0002t0001g0190others(148): Show | 161 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(158): Show |
intron_variant | MODIFIER | c.1170+1286T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246531 | ||||||
chr6:139246577
|
C | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1240G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246577 | ||||||
chr6:139246639
|
G | T | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+1178C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246639 | ||||||
chr6:139246783
|
G | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+1034C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246783 | ||||||
chr6:139246907
|
T | C | 126 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(123): Show | 136 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(133): Show |
intron_variant | MODIFIER | c.1170+910A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246907 | ||||||
chr6:139246914
|
C | CA | 22 | a0002c0002t0003g0185a0003c0003t0004g0064a0003c0003t0004g0080others(19): Show | 22 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1170+902dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246914 | ||||||
chr6:139246914
|
CA | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0138a0002c0002t0001g0190others(9): Show | 12 | HG00639.hp1 HG01169.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1170+902delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246914 | ||||||
chr6:139246985
|
C | T | 7 | a0003c0008t0002g0245a0004c0005t0002g0141a0004c0005t0002g0143others(4): Show | 7 | HG01081.hp1 HG01106.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+832G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246985 | ||||||
chr6:139247170
|
T | G | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+647A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247170 | ||||||
chr6:139247174
|
G | A | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170+643C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247174 | ||||||
chr6:139247203
|
C | T | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+614G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247203 | ||||||
chr6:139247227
|
T | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+590A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247227 | ||||||
chr6:139247244
|
C | T | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+573G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247244 | ||||||
chr6:139247299
|
G | A | 2 | a0001c0001t0001g0131a0008c0015t0011g0255 | 2 | HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1170+518C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247299 | ||||||
chr6:139247383
|
T | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+434A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247383 | ||||||
chr6:139247529
|
CTTCTTTT others(36): Show |
C | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170+245_1170+287d others(45): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247529 | ||||||
chr6:139247532
|
C | CT | 15 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0045others(12): Show | 16 | HG00558.hp2 HG01243.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+284dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | ||||||
chr6:139247532
|
CT | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0039others(57): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1170+284delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | ||||||
chr6:139247532
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1170+269_1170+284d others(18): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | ||||||
chr6:139247618
|
T | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+199A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247618 | ||||||
chr6:139247945
|
C | T | 1 | a0009c0032t0028g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1078-36G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139247945 | ||||||
chr6:139248049
|
G | C | 3 | a0006c0007t0005g0176a0006c0007t0005g0180a0012c0033t0020g0162 | 3 | HG01884.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1078-140C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248049 | ||||||
chr6:139248056
|
T | C | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-147A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248056 | ||||||
chr6:139248186
|
T | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-277A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248186 | ||||||
chr6:139248222
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0077a0010c0021t0001g0020 | 3 | HG01257.hp1 HG01261.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1078-313C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248222 | ||||||
chr6:139248237
|
T | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-328A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248237 | ||||||
chr6:139248272
|
C | CA | 11 | a0001c0001t0001g0073a0001c0001t0003g0117a0001c0001t0015g0040others(8): Show | 12 | HG01175.hp2 HG02074.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1078-364dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248272 | ||||||
chr6:139248272
|
CA | C | 21 | a0002c0002t0001g0221a0003c0003t0004g0064a0003c0003t0004g0080others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-364delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248272 | ||||||
chr6:139248303
|
C | G | 5 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-394G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248303 | ||||||
chr6:139248324
|
C | T | 2 | a0002c0016t0006g0150a0002c0016t0006g0151 | 2 | HG00558.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1078-415G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248324 | ||||||
chr6:139248371
|
C | T | 2 | a0008c0015t0011g0254a0008c0015t0011g0255 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1078-462G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248371 | ||||||
chr6:139248387
|
T | C | 119 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(116): Show | 129 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(126): Show |
intron_variant | MODIFIER | c.1078-478A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248387 | ||||||
chr6:139248497
|
C | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1078-588G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248497 | ||||||
chr6:139248530
|
T | C | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-621A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248530 | ||||||
chr6:139248632
|
G | T | 1 | a0002c0002t0003g0225 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1078-723C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248632 | ||||||
chr6:139248696
|
G | A | 82 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(79): Show | 92 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.1078-787C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248696 | ||||||
chr6:139248724
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1078-815G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248724 | ||||||
chr6:139249024
|
G | C | 21 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(18): Show | 21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-1115C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249024 | ||||||
chr6:139249127
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-1218C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249127 | ||||||
chr6:139249159
|
A | C | 156 | a0001c0001t0001g0133a0001c0001t0024g0139a0002c0002t0001g0190others(153): Show | 166 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.1078-1250T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249159 | ||||||
chr6:139249428
|
T | G | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-1519A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249428 | ||||||
chr6:139249455
|
C | T | 1 | a0002c0002t0003g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1078-1546G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249455 | ||||||
chr6:139249565
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1078-1656G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249565 | ||||||
chr6:139249619
|
G | A | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-1710C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249619 | ||||||
chr6:139249639
|
G | A | 17 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(14): Show | 17 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-1730C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249639 | ||||||
chr6:139249949
|
G | A | 119 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(116): Show | 129 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(126): Show |
intron_variant | MODIFIER | c.1078-2040C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249949 | ||||||
chr6:139249983
|
C | T | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-2074G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249983 | ||||||
chr6:139250003
|
G | A | 154 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(151): Show | 164 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.1078-2094C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250003 | ||||||
chr6:139250084
|
A | C | 1 | a0002c0009t0002g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-2175T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250084 | ||||||
chr6:139250177
|
C | CT | 6 | a0002c0002t0006g0069a0003c0011t0005g0046a0003c0011t0019g0116others(3): Show | 6 | HG02809.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-2269dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | ||||||
chr6:139250177
|
C | CTT | 27 | a0002c0016t0006g0150a0002c0016t0006g0151a0003c0003t0004g0064others(24): Show | 27 | HG00323.hp2 HG00558.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1078-2270_1078-226 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | ||||||
chr6:139250177
|
CT | C | 86 | a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0024g0139others(83): Show | 96 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1078-2269delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | ||||||
chr6:139250177
|
CTT | C | 9 | a0002c0002t0003g0208a0003c0008t0008g0111a0003c0008t0008g0189others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-2270_1078-226 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | ||||||
chr6:139250177
|
CTTT | C | 6 | a0003c0008t0002g0245a0004c0005t0002g0141a0004c0005t0002g0143others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-2271_1078-226 others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | ||||||
chr6:139250217
|
C | T | 1 | a0002c0002t0003g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1078-2308G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250217 | ||||||
chr6:139250218
|
G | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1078-2309C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250218 | ||||||
chr6:139250357
|
C | CT | 26 | a0001c0001t0001g0100a0001c0001t0001g0123a0001c0001t0001g0127others(23): Show | 26 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1078-2449dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250357 | ||||||
chr6:139250357
|
CT | C | 81 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0102others(78): Show | 91 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.1078-2449delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250357 | ||||||
chr6:139250358
|
T | TTTC | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-2450_1078-244 others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250358 | ||||||
chr6:139250523
|
G | T | 5 | a0003c0003t0004g0148a0003c0003t0004g0153a0003c0003t0004g0193others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-2614C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250523 | ||||||
chr6:139250529
|
A | C | 1 | a0013c0026t0025g0211 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1078-2620T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250529 | ||||||
chr6:139250577
|
T | C | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-2668A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250577 | ||||||
chr6:139250871
|
G | A | 1 | a0002c0002t0007g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1078-2962C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250871 | ||||||
chr6:139251283
|
G | A | 85 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(82): Show | 95 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1078-3374C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251283 | ||||||
chr6:139251397
|
G | C | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-3488C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251397 | ||||||
chr6:139251508
|
C | T | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-3599G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251508 | ||||||
chr6:139251532
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1078-3623T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251532 | ||||||
chr6:139251568
|
T | C | 17 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(14): Show | 17 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-3659A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251568 | ||||||
chr6:139251587
|
G | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-3678C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251587 | ||||||
chr6:139251771
|
G | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+3793C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251771 | ||||||
chr6:139251877
|
G | C | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+3687C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251877 | ||||||
chr6:139251977
|
A | C | 15 | a0003c0008t0001g0192a0003c0008t0002g0245a0003c0008t0008g0111others(12): Show | 15 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+3587T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251977 | ||||||
chr6:139252033
|
C | T | 6 | a0003c0008t0002g0245a0004c0005t0002g0141a0004c0005t0002g0143others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+3531G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252033 | ||||||
chr6:139252039
|
A | AT | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+3524dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252039 | ||||||
chr6:139252162
|
G | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+3402C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252162 | ||||||
chr6:139252292
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1077+3272G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252292 | ||||||
chr6:139252355
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1077+3209T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252355 | ||||||
chr6:139252501
|
A | C | 1 | a0001c0001t0001g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1077+3063T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252501 | ||||||
chr6:139252774
|
G | A | 1 | a0002c0002t0002g0239 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1077+2790C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252774 | ||||||
chr6:139252916
|
C | T | 119 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(116): Show | 129 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(126): Show |
intron_variant | MODIFIER | c.1077+2648G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252916 | ||||||
chr6:139252951
|
C | A | 2 | a0001c0001t0015g0040a0001c0001t0015g0067 | 2 | HG00597.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1077+2613G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252951 | ||||||
chr6:139252982
|
A | T | 1 | a0001c0004t0001g0005 | 3 | NA18956.hp2 NA18995.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1077+2582T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252982 | ||||||
chr6:139252997
|
C | T | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+2567G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252997 | ||||||
chr6:139253077
|
A | C | 1 | a0003c0003t0004g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+2487T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253077 | ||||||
chr6:139253233
|
G | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+2331C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253233 | ||||||
chr6:139253246
|
G | C | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2318C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253246 | ||||||
chr6:139253317
|
A | G | 3 | a0004c0006t0005g0256a0004c0006t0005g0258a0004c0017t0005g0257 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1077+2247T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253317 | ||||||
chr6:139253365
|
C | T | 3 | a0003c0008t0002g0175a0003c0031t0022g0242a0017c0020t0002g0252 | 3 | HG01243.hp1 HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1077+2199G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253365 | ||||||
chr6:139253421
|
A | G | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2143T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253421 | ||||||
chr6:139253456
|
C | T | 1 | a0004c0005t0002g0143 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1077+2108G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253456 | ||||||
chr6:139253457
|
G | A | 3 | a0005c0010t0005g0181a0005c0013t0010g0119a0005c0013t0010g0160 | 3 | HG03225.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1077+2107C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253457 | ||||||
chr6:139253524
|
T | C | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1077+2040A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253524 | ||||||
chr6:139253563
|
C | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2001G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253563 | ||||||
chr6:139253627
|
A | G | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1937T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253627 | ||||||
chr6:139253685
|
A | G | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1077+1879T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253685 | ||||||
chr6:139253734
|
T | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1830A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253734 | ||||||
chr6:139253773
|
A | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0085a0001c0004t0001g0003others(6): Show | 15 | HG00673.hp1 HG02040.hp2 NA18956.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+1791T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253773 | ||||||
chr6:139253804
|
G | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+1760C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253804 | ||||||
chr6:139253887
|
C | G | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+1677G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253887 | ||||||
chr6:139253927
|
T | G | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+1637A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253927 | ||||||
chr6:139254026
|
G | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1538C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254026 | ||||||
chr6:139254026
|
G | T | 6 | a0003c0012t0005g0168a0003c0012t0005g0170a0003c0012t0005g0171others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+1538C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254026 | ||||||
chr6:139254192
|
A | G | 1 | a0003c0003t0004g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+1372T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254192 | ||||||
chr6:139254223
|
A | G | 1 | a0003c0014t0008g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1077+1341T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254223 | ||||||
chr6:139254311
|
C | T | 2 | a0003c0003t0004g0193a0003c0003t0004g0194 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1077+1253G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254311 | ||||||
chr6:139254315
|
T | G | 1 | a0002c0002t0003g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+1249A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTG | 15 | a0001c0001t0001g0007a0001c0001t0001g0125a0003c0003t0004g0148others(12): Show | 16 | HG01109.hp2 HG01978.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+1247_1077+124 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTG | 7 | a0002c0002t0002g0182a0002c0002t0002g0200a0002c0002t0002g0223others(4): Show | 7 | HG01433.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+1245_1077+124 others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTG | 3 | a0002c0002t0002g0212a0002c0002t0002g0229a0011c0022t0005g0014 | 3 | HG00639.hp1 HG02809.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1077+1243_1077+124 others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTGT others(1): Show |
76 | a0001c0001t0001g0133a0001c0001t0024g0139a0002c0002t0001g0190others(73): Show | 86 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.1077+1241_1077+124 others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTGT others(3): Show |
21 | a0002c0002t0002g0222a0002c0002t0003g0186a0002c0002t0003g0218others(18): Show | 21 | HG00735.hp1 HG01106.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1077+1239_1077+124 others(14): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTGT others(5): Show |
9 | a0002c0002t0003g0023a0003c0008t0002g0245a0003c0031t0022g0242others(6): Show | 9 | HG00733.hp1 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077+1237_1077+124 others(16): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTGT others(9): Show |
1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077+1233_1077+124 others(20): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
T | TTGTGTGT others(11): Show |
1 | a0017c0020t0002g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1077+1231_1077+124 others(22): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254315
|
TTG | T | 3 | a0003c0003t0004g0193a0003c0003t0004g0194a0003c0003t0016g0149 | 3 | HG02109.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1077+1247_1077+124 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | ||||||
chr6:139254715
|
C | T | 154 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(151): Show | 164 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.1077+849G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254715 | ||||||
chr6:139254747
|
A | AT | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1077+816dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254747 | ||||||
chr6:139254781
|
G | T | 1 | a0001c0001t0001g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1077+783C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254781 | ||||||
chr6:139254784
|
T | A | 1 | a0002c0002t0001g0030 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1077+780A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254784 | ||||||
chr6:139254827
|
T | G | 1 | a0002c0009t0005g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1077+737A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254827 | ||||||
chr6:139254878
|
A | G | 156 | a0001c0001t0001g0133a0001c0001t0024g0139a0002c0002t0001g0190others(153): Show | 166 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.1077+686T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254878 | ||||||
chr6:139254975
|
C | T | 1 | a0002c0002t0003g0269 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1077+589G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254975 | ||||||
chr6:139255041
|
C | T | 15 | a0003c0011t0005g0046a0003c0011t0005g0121a0003c0011t0018g0152others(12): Show | 15 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+523G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255041 | ||||||
chr6:139255060
|
G | A | 1 | a0013c0026t0025g0211 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1077+504C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255060 | ||||||
chr6:139255118
|
G | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+446C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255118 | ||||||
chr6:139255356
|
C | T | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+208G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255356 | ||||||
chr6:139255357
|
G | A | 1 | a0003c0011t0019g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1077+207C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255357 | ||||||
chr6:139255407
|
G | A | 67 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(64): Show | 67 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.1077+157C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255407 | ||||||
chr6:139255513
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1077+51T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255513 | ||||||
chr6:139255642
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA18988.hp2 | splice_region_variant&intron_variant | LOW | c.1003-4A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255642 | ||||||
chr6:139255669
|
G | T | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-31C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255669 | ||||||
chr6:139255898
|
G | A | 2 | a0002c0009t0002g0163a0002c0009t0002g0174 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1003-260C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255898 | ||||||
chr6:139255912
|
G | GA | 13 | a0001c0001t0003g0117a0002c0002t0001g0221a0002c0002t0003g0220others(10): Show | 13 | HG01175.hp1 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1003-275dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255912 | ||||||
chr6:139255927
|
C | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0002c0002t0003g0026others(9): Show | 12 | HG00642.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1003-289G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255927 | ||||||
chr6:139256063
|
T | C | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1003-425A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256063 | ||||||
chr6:139256207
|
A | T | 3 | a0002c0002t0006g0009a0002c0002t0006g0048a0002c0002t0006g0084 | 4 | HG00438.hp1 NA18960.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-569T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256207 | ||||||
chr6:139256569
|
C | G | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-931G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256569 | ||||||
chr6:139256603
|
T | C | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-965A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256603 | ||||||
chr6:139256618
|
G | A | 8 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1003-980C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256618 | ||||||
chr6:139256623
|
C | A | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1003-985G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256623 | ||||||
chr6:139256703
|
A | G | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1003-1065T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256703 | ||||||
chr6:139256850
|
A | G | 1 | a0004c0006t0005g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1003-1212T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256850 | ||||||
chr6:139257243
|
T | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1003-1605A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257243 | ||||||
chr6:139257477
|
G | A | 8 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1003-1839C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257477 | ||||||
chr6:139257477
|
G | T | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1003-1839C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257477 | ||||||
chr6:139257560
|
T | C | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1003-1922A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257560 | ||||||
chr6:139257572
|
T | C | 83 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(80): Show | 93 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.1003-1934A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257572 | ||||||
chr6:139257645
|
G | A | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1003-2007C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257645 | ||||||
chr6:139257724
|
T | TA | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1003-2087dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257724 | ||||||
chr6:139257789
|
T | C | 1 | a0002c0002t0003g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1003-2151A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257789 | ||||||
chr6:139257872
|
G | T | 83 | a0001c0001t0024g0139a0002c0002t0001g0190a0002c0002t0001g0191others(80): Show | 93 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.1003-2234C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257872 | ||||||
chr6:139258263
|
G | A | 6 | a0002c0002t0003g0023a0002c0002t0007g0024a0002c0002t0007g0025others(3): Show | 6 | HG00733.hp1 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+2055C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258263 | ||||||
chr6:139258327
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1002+1991T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258327 | ||||||
chr6:139258362
|
A | G | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1002+1956T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258362 | ||||||
chr6:139258412
|
C | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1002+1906G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258412 | ||||||
chr6:139258414
|
A | G | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002+1904T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258414 | ||||||
chr6:139258622
|
C | T | 154 | a0001c0001t0024g0139a0001c0028t0001g0015a0002c0002t0001g0190others(151): Show | 164 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.1002+1696G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258622 | ||||||
chr6:139258742
|
A | C | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1002+1576T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258742 | ||||||
chr6:139258749
|
C | T | 1 | a0013c0026t0025g0211 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1002+1569G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258749 | ||||||
chr6:139258750
|
G | A | 3 | a0002c0002t0003g0004a0002c0002t0003g0185a0002c0002t0003g0205 | 5 | HG01261.hp2 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1568C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258750 | ||||||
chr6:139258798
|
A | C | 1 | a0003c0003t0004g0197 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002+1520T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258798 | ||||||
chr6:139259018
|
T | C | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1002+1300A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259018 | ||||||
chr6:139259101
|
C | T | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+1217G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259101 | ||||||
chr6:139259102
|
A | G | 1 | a0003c0003t0004g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1002+1216T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259102 | ||||||
chr6:139259176
|
G | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1002+1142C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259176 | ||||||
chr6:139259348
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1002+970C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259348 | ||||||
chr6:139259459
|
C | T | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002+859G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259459 | ||||||
chr6:139259488
|
G | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+830C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259488 | ||||||
chr6:139259655
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 236 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1002+663G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259655 | ||||||
chr6:139259860
|
T | C | 37 | a0001c0001t0001g0133a0003c0008t0001g0192a0003c0008t0002g0175others(34): Show | 37 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1002+458A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259860 | ||||||
chr6:139259957
|
T | A | 2 | a0002c0002t0002g0200a0002c0002t0002g0223 | 2 | HG01433.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1002+361A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259957 | ||||||
chr6:139259979
|
T | C | 1 | a0003c0031t0022g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1002+339A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259979 | ||||||
chr6:139259998
|
G | A | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1002+320C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259998 | ||||||
chr6:139260122
|
A | T | 16 | a0001c0001t0001g0133a0003c0011t0005g0046a0003c0011t0005g0121others(13): Show | 16 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002+196T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260122 | ||||||
chr6:139260136
|
C | T | 1 | a0002c0025t0003g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1002+182G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260136 | ||||||
chr6:139260219
|
C | CAAAT | 15 | a0001c0028t0001g0015a0002c0002t0003g0159a0002c0016t0006g0150others(12): Show | 15 | HG00558.hp1 HG02055.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002+95_1002+98dup others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260219 | ||||||
chr6:139260267
|
C | G | 1 | a0003c0011t0005g0121 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1002+51G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260267 | ||||||
chr6:139260670
|
A | T | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883-233T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139260670 | ||||||
chr6:139260967
|
C | G | 1 | a0002c0009t0002g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.883-530G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139260967 | ||||||
chr6:139261289
|
T | C | 1 | a0004c0005t0002g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.883-852A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261289 | ||||||
chr6:139261329
|
A | AGATAAAA others(2): Show |
3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.883-901_883-893dup others(9): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261329 | ||||||
chr6:139261348
|
C | T | 2 | a0002c0002t0001g0210a0002c0002t0001g0221 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.883-911G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261348 | ||||||
chr6:139261828
|
G | T | 14 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(11): Show | 14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+751C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261828 | ||||||
chr6:139261901
|
C | CT | 113 | a0001c0001t0001g0018a0001c0001t0001g0133a0001c0001t0003g0117others(110): Show | 123 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.882+677dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | ||||||
chr6:139261901
|
C | CTT | 13 | a0001c0001t0024g0139a0002c0002t0002g0222a0002c0002t0003g0079others(10): Show | 13 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+676_882+677dup others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | ||||||
chr6:139261901
|
CT | C | 12 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0107others(9): Show | 12 | HG01257.hp2 HG01975.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+677delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | ||||||
chr6:139262049
|
G | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.882+530C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262049 | ||||||
chr6:139262070
|
A | AT | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+508dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262070 | ||||||
chr6:139262088
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+491T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262088 | ||||||
chr6:139262257
|
G | A | 1 | a0003c0003t0004g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882+322C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262257 | ||||||
chr6:139262330
|
C | T | 2 | a0005c0010t0005g0181a0012c0033t0020g0162 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.882+249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262330 | ||||||
chr6:139262446
|
G | A | 1 | a0003c0003t0004g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+133C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262446 | ||||||
chr6:139262452
|
G | A | 1 | a0003c0011t0018g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+127C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262452 | ||||||
chr6:139262777
|
C | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0052 | 2 | HG01099.hp2 HG01515.hp2 |
splice_region_variant&intron_variant | LOW | c.688-4G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262777 | ||||||
chr6:139262821
|
T | C | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-48A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262821 | ||||||
chr6:139262853
|
A | T | 155 | a0001c0001t0001g0133a0001c0001t0024g0139a0001c0028t0001g0015others(152): Show | 165 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.688-80T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262853 | ||||||
chr6:139262911
|
C | T | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-138G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262911 | ||||||
chr6:139263029
|
C | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.688-256G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263029 | ||||||
chr6:139263121
|
A | C | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-348T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263121 | ||||||
chr6:139263280
|
A | C | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-507T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263280 | ||||||
chr6:139263414
|
A | C | 1 | a0002c0002t0002g0054 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.688-641T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263414 | ||||||
chr6:139263477
|
A | G | 2 | a0003c0011t0005g0046a0003c0011t0019g0116 | 2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.688-704T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263477 | ||||||
chr6:139263511
|
G | A | 9 | a0003c0011t0005g0121a0003c0012t0005g0168a0003c0012t0005g0170others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.688-738C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263511 | ||||||
chr6:139263535
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.688-762C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263535 | ||||||
chr6:139263681
|
G | GTTATTC | 155 | a0001c0001t0024g0139a0001c0028t0001g0015a0002c0002t0001g0190others(152): Show | 165 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.688-914_688-909dup others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263681 | ||||||
chr6:139263696
|
TA | T | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-924delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263696 | ||||||
chr6:139264000
|
A | G | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688-1227T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264000 | ||||||
chr6:139264244
|
G | A | 2 | a0003c0008t0002g0175a0003c0031t0022g0242 | 2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.688-1471C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264244 | ||||||
chr6:139264336
|
T | C | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.688-1563A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264336 | ||||||
chr6:139264413
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0127 | 2 | NA19010.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.688-1640A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264413 | ||||||
chr6:139264478
|
T | A | 3 | a0003c0003t0004g0193a0003c0003t0004g0194a0012c0033t0020g0162 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.688-1705A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264478 | ||||||
chr6:139264541
|
A | T | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-1768T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264541 | ||||||
chr6:139264543
|
T | A | 1 | a0003c0011t0018g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.688-1770A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | ||||||
chr6:139264543
|
T | TTTTTG | 62 | a0001c0001t0001g0133a0001c0001t0024g0139a0002c0002t0001g0190others(59): Show | 70 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.688-1775_688-1771d others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | ||||||
chr6:139264543
|
T | TTTTTGTT others(3): Show |
3 | a0002c0002t0002g0074a0002c0002t0002g0184a0006c0018t0016g0177 | 3 | HG01433.hp1 HG03139.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.688-1780_688-1771d others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | ||||||
chr6:139264548
|
G | GTT | 8 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-1777_688-1776d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264548 | ||||||
chr6:139264707
|
G | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688-1934C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264707 | ||||||
chr6:139264748
|
C | T | 1 | a0002c0002t0003g0206 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.688-1975G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264748 | ||||||
chr6:139264815
|
C | T | 7 | a0002c0002t0003g0159a0002c0002t0003g0206a0002c0002t0003g0207others(4): Show | 7 | HG02165.hp2 HG03688.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-2042G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264815 | ||||||
chr6:139265066
|
G | A | 2 | a0002c0002t0002g0182a0002c0009t0005g0172 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.688-2293C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265066 | ||||||
chr6:139265143
|
A | G | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-2370T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265143 | ||||||
chr6:139265426
|
A | ATG | 19 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.688-2655_688-2654d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265426 | ||||||
chr6:139265446
|
C | CTG | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0202others(3): Show | 6 | HG02135.hp1 HG02698.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.688-2675_688-2674d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265446 | ||||||
chr6:139265456
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.688-2683C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265456 | ||||||
chr6:139265483
|
C | T | 7 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-2710G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265483 | ||||||
chr6:139265517
|
G | A | 15 | a0002c0002t0003g0004a0002c0002t0003g0023a0002c0002t0003g0026others(12): Show | 17 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.688-2744C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265517 | ||||||
chr6:139265578
|
T | C | 18 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(15): Show | 18 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.688-2805A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265578 | ||||||
chr6:139265632
|
T | G | 7 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-2859A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265632 | ||||||
chr6:139265742
|
T | C | 8 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-2969A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265742 | ||||||
chr6:139266288
|
T | A | 2 | a0003c0011t0005g0046a0003c0011t0019g0116 | 2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.688-3515A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266288 | ||||||
chr6:139266340
|
A | C | 1 | a0002c0025t0003g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.688-3567T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266340 | ||||||
chr6:139266590
|
C | T | 4 | a0002c0002t0003g0240a0002c0009t0002g0167a0006c0007t0002g0261others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-3817G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266590 | ||||||
chr6:139266623
|
A | G | 1 | a0002c0002t0006g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.687+3833T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266623 | ||||||
chr6:139266656
|
A | G | 1 | a0002c0002t0032g0270 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.687+3800T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266656 | ||||||
chr6:139266824
|
C | T | 1 | a0003c0003t0004g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.687+3632G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266824 | ||||||
chr6:139266880
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.687+3576C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266880 | ||||||
chr6:139266951
|
T | C | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+3505A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266951 | ||||||
chr6:139266965
|
G | GA | 82 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0063others(79): Show | 92 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.687+3490dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | ||||||
chr6:139266965
|
G | GAA | 49 | a0001c0001t0001g0133a0001c0028t0001g0015a0002c0002t0002g0034others(46): Show | 49 | HG00558.hp1 HG01081.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.687+3489_687+3490d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | ||||||
chr6:139266965
|
G | GAAA | 10 | a0003c0008t0001g0192a0003c0008t0008g0111a0003c0008t0008g0189others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+3488_687+3490d others(5): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | ||||||
chr6:139267039
|
TA | T | 14 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(11): Show | 14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+3416delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267039 | ||||||
chr6:139267073
|
G | A | 19 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+3383C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267073 | ||||||
chr6:139267207
|
A | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0125others(5): Show | 9 | HG00673.hp2 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.687+3249T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267207 | ||||||
chr6:139267223
|
G | C | 19 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+3233C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267223 | ||||||
chr6:139267616
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.687+2840G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267616 | ||||||
chr6:139267626
|
A | G | 1 | a0003c0008t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687+2830T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267626 | ||||||
chr6:139267814
|
A | G | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+2642T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267814 | ||||||
chr6:139267878
|
C | A | 14 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(11): Show | 14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+2578G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267878 | ||||||
chr6:139267923
|
C | T | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.687+2533G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267923 | ||||||
chr6:139268075
|
G | A | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+2381C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268075 | ||||||
chr6:139268109
|
C | T | 1 | a0002c0002t0002g0239 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.687+2347G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268109 | ||||||
chr6:139268151
|
C | CA | 33 | a0001c0001t0001g0053a0001c0001t0001g0063a0001c0001t0001g0090others(30): Show | 34 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.687+2304dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | ||||||
chr6:139268151
|
C | CAA | 20 | a0001c0001t0001g0133a0002c0002t0003g0240a0002c0009t0002g0167others(17): Show | 20 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+2303_687+2304d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | ||||||
chr6:139268151
|
CA | C | 17 | a0003c0003t0004g0080a0003c0003t0004g0112a0003c0003t0004g0148others(14): Show | 17 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.687+2304delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | ||||||
chr6:139268261
|
G | C | 2 | a0008c0015t0011g0254a0008c0015t0011g0255 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.687+2195C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268261 | ||||||
chr6:139268322
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.687+2134A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268322 | ||||||
chr6:139268444
|
T | C | 19 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+2012A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268444 | ||||||
chr6:139268563
|
A | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+1893T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268563 | ||||||
chr6:139268822
|
G | A | 1 | a0002c0002t0003g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.687+1634C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268822 | ||||||
chr6:139268846
|
T | C | 1 | a0003c0011t0019g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.687+1610A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268846 | ||||||
chr6:139268897
|
T | C | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687+1559A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268897 | ||||||
chr6:139268908
|
C | T | 145 | a0001c0001t0024g0139a0001c0028t0001g0015a0002c0002t0001g0190others(142): Show | 155 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.687+1548G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268908 | ||||||
chr6:139268970
|
A | T | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.687+1486T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268970 | ||||||
chr6:139268996
|
C | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+1460G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268996 | ||||||
chr6:139269031
|
C | T | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.687+1425G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269031 | ||||||
chr6:139269089
|
T | C | 69 | a0002c0002t0003g0240a0002c0009t0002g0167a0003c0003t0004g0064others(66): Show | 69 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.687+1367A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269089 | ||||||
chr6:139269125
|
G | A | 14 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(11): Show | 14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+1331C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269125 | ||||||
chr6:139269295
|
C | T | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.687+1161G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269295 | ||||||
chr6:139269318
|
T | G | 2 | a0003c0011t0005g0046a0003c0011t0019g0116 | 2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.687+1138A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269318 | ||||||
chr6:139269403
|
C | T | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.687+1053G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269403 | ||||||
chr6:139269404
|
G | A | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+1052C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269404 | ||||||
chr6:139269780
|
G | A | 1 | a0012c0033t0020g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.687+676C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269780 | ||||||
chr6:139269902
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.687+554A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269902 | ||||||
chr6:139269988
|
G | T | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687+468C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269988 | ||||||
chr6:139270018
|
C | T | 1 | a0003c0031t0022g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.687+438G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270018 | ||||||
chr6:139270065
|
CAAAAATG others(3): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.687+381_687+390del others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270065 | ||||||
chr6:139270088
|
T | C | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+368A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270088 | ||||||
chr6:139270201
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.687+255C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270201 | ||||||
chr6:139270368
|
TA | T | 77 | a0001c0001t0001g0226a0001c0001t0024g0139a0001c0028t0001g0015others(74): Show | 87 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.687+87delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270368 | ||||||
chr6:139270709
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-83T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270709 | ||||||
chr6:139270710
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-84G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270710 | ||||||
chr6:139270712
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-86G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270712 | ||||||
chr6:139270714
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-88C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270714 | ||||||
chr6:139270715
|
T | A | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-89A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270715 | ||||||
chr6:139270716
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-90C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270716 | ||||||
chr6:139270717
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-91C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270717 | ||||||
chr6:139270720
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-94C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270720 | ||||||
chr6:139270724
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-98C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270724 | ||||||
chr6:139270725
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-99C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270725 | ||||||
chr6:139270726
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-100T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270726 | ||||||
chr6:139270727
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-101T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270727 | ||||||
chr6:139270729
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-103G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270729 | ||||||
chr6:139270737
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-111C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270737 | ||||||
chr6:139270738
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-112G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270738 | ||||||
chr6:139270740
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-114T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270740 | ||||||
chr6:139270741
|
T | A | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-115A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270741 | ||||||
chr6:139270743
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-117T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270743 | ||||||
chr6:139270745
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-119G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270745 | ||||||
chr6:139270747
|
C | T | 2 | a0002c0009t0002g0163a0011c0022t0005g0014 | 2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517-121G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270747 | ||||||
chr6:139270750
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-124G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270750 | ||||||
chr6:139270751
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-125G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270751 | ||||||
chr6:139270753
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-127G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270753 | ||||||
chr6:139270754
|
T | C | 8 | a0002c0002t0003g0004a0002c0002t0003g0026a0002c0002t0003g0079others(5): Show | 10 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-128A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270754 | ||||||
chr6:139270755
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-129C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270755 | ||||||
chr6:139270756
|
G | C | 1 | a0002c0002t0003g0225 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.517-130C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270756 | ||||||
chr6:139270756
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-130C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270756 | ||||||
chr6:139270757
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-131T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270757 | ||||||
chr6:139270758
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-132T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270758 | ||||||
chr6:139270759
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-133C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270759 | ||||||
chr6:139270761
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-135T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270761 | ||||||
chr6:139270762
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-136T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270762 | ||||||
chr6:139270763
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-137T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270763 | ||||||
chr6:139270765
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-139C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270765 | ||||||
chr6:139270766
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-140T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270766 | ||||||
chr6:139270767
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-141T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270767 | ||||||
chr6:139270768
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-142T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270768 | ||||||
chr6:139270771
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-145G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270771 | ||||||
chr6:139270772
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-146T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270772 | ||||||
chr6:139270773
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-147G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270773 | ||||||
chr6:139270774
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-148T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270774 | ||||||
chr6:139270775
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-149T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270775 | ||||||
chr6:139270776
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-150T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270776 | ||||||
chr6:139270777
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-151G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270777 | ||||||
chr6:139270778
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0001g0118 | 3 | HG01243.hp2 NA18966.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.517-152C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270778 | ||||||
chr6:139270778
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-152C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270778 | ||||||
chr6:139270780
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-154G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270780 | ||||||
chr6:139270781
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-155T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270781 | ||||||
chr6:139270782
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-156G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270782 | ||||||
chr6:139270783
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-157G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270783 | ||||||
chr6:139270787
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-161C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270787 | ||||||
chr6:139270789
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-163T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270789 | ||||||
chr6:139270790
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-164C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270790 | ||||||
chr6:139270792
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-166T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270792 | ||||||
chr6:139270793
|
C | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-167G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270793 | ||||||
chr6:139270796
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-170C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270796 | ||||||
chr6:139270797
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-171T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270797 | ||||||
chr6:139270798
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-172T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270798 | ||||||
chr6:139270799
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-173C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270799 | ||||||
chr6:139270800
|
G | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-174C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270800 | ||||||
chr6:139270802
|
A | T | 1 | a0002c0009t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-176T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270802 | ||||||
chr6:139270979
|
G | A | 1 | a0002c0002t0002g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.517-353C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270979 | ||||||
chr6:139271004
|
T | A | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-378A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271004 | ||||||
chr6:139271055
|
C | G | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-429G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271055 | ||||||
chr6:139271066
|
C | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.517-440G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271066 | ||||||
chr6:139271139
|
G | T | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.517-513C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271139 | ||||||
chr6:139271276
|
T | A | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517-650A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271276 | ||||||
chr6:139271444
|
C | T | 1 | a0004c0005t0002g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.517-818G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271444 | ||||||
chr6:139271527
|
A | G | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.517-901T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271527 | ||||||
chr6:139271675
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-1049A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271675 | ||||||
chr6:139271734
|
G | T | 61 | a0001c0001t0001g0226a0001c0001t0024g0139a0002c0002t0001g0190others(58): Show | 69 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.517-1108C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271734 | ||||||
chr6:139271745
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.517-1119A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271745 | ||||||
chr6:139271991
|
C | T | 14 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(11): Show | 14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-1365G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271991 | ||||||
chr6:139272029
|
C | T | 1 | a0004c0017t0005g0257 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.517-1403G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272029 | ||||||
chr6:139272188
|
T | A | 1 | a0002c0002t0003g0247 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.517-1562A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272188 | ||||||
chr6:139272271
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-1645G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272271 | ||||||
chr6:139272272
|
G | A | 18 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(15): Show | 18 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.517-1646C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272272 | ||||||
chr6:139272384
|
G | A | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-1758C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272384 | ||||||
chr6:139272617
|
C | A | 5 | a0005c0010t0013g0154a0005c0010t0013g0155a0005c0010t0014g0156others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-1991G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272617 | ||||||
chr6:139272635
|
T | C | 74 | a0001c0001t0001g0092a0001c0001t0001g0226a0001c0001t0024g0139others(71): Show | 84 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.517-2009A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272635 | ||||||
chr6:139272902
|
C | T | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2276G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272902 | ||||||
chr6:139272903
|
G | A | 19 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0008t0002g0245others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-2277C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272903 | ||||||
chr6:139273012
|
T | C | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2386A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273012 | ||||||
chr6:139273013
|
G | A | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2387C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273013 | ||||||
chr6:139273216
|
C | G | 15 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-2590G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273216 | ||||||
chr6:139273309
|
C | T | 4 | a0002c0002t0003g0240a0002c0009t0002g0167a0006c0007t0002g0261others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2683G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273309 | ||||||
chr6:139273353
|
T | C | 1 | a0005c0013t0010g0119 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-2727A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273353 | ||||||
chr6:139273403
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.517-2777T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273403 | ||||||
chr6:139273454
|
T | C | 1 | a0003c0011t0018g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-2828A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273454 | ||||||
chr6:139273554
|
C | T | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2928G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273554 | ||||||
chr6:139273595
|
GCTGGGA | G | 3 | a0002c0002t0003g0004a0002c0002t0003g0185a0002c0002t0003g0205 | 5 | HG01261.hp2 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-2975_517-2970d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273595 | ||||||
chr6:139273626
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0081 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-3000T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273626 | ||||||
chr6:139274502
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.516+2328C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274502 | ||||||
chr6:139274586
|
T | A | 1 | a0016c0029t0002g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516+2244A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274586 | ||||||
chr6:139274659
|
C | G | 10 | a0003c0011t0005g0121a0003c0011t0018g0152a0003c0012t0005g0168others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+2171G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274659 | ||||||
chr6:139274685
|
G | A | 3 | a0005c0013t0010g0119a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.516+2145C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274685 | ||||||
chr6:139274718
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.516+2112G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274718 | ||||||
chr6:139274775
|
C | T | 15 | a0003c0008t0001g0192a0003c0008t0002g0245a0003c0008t0008g0111others(12): Show | 15 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.516+2055G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274775 | ||||||
chr6:139274834
|
T | C | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516+1996A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274834 | ||||||
chr6:139274913
|
C | T | 24 | a0003c0008t0002g0245a0003c0008t0008g0111a0003c0008t0008g0189others(21): Show | 24 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.516+1917G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274913 | ||||||
chr6:139275156
|
T | C | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516+1674A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275156 | ||||||
chr6:139275249
|
T | A | 1 | a0003c0014t0008g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.516+1581A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275249 | ||||||
chr6:139275299
|
C | A | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+1531G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275299 | ||||||
chr6:139275482
|
T | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | NA18960.hp2 NA18995.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1348A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275482 | ||||||
chr6:139275547
|
T | A | 6 | a0003c0008t0001g0192a0003c0008t0002g0175a0003c0031t0022g0242others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1283A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275547 | ||||||
chr6:139275644
|
G | A | 25 | a0002c0009t0005g0172a0003c0008t0002g0245a0003c0008t0008g0111others(22): Show | 25 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+1186C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275644 | ||||||
chr6:139275872
|
C | T | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+958G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275872 | ||||||
chr6:139275891
|
A | G | 14 | a0002c0002t0003g0240a0002c0009t0002g0167a0004c0006t0005g0256others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+939T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275891 | ||||||
chr6:139276075
|
T | C | 1 | a0015c0024t0027g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.516+755A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276075 | ||||||
chr6:139276127
|
A | G | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+703T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276127 | ||||||
chr6:139276256
|
C | T | 1 | a0002c0009t0005g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516+574G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276256 | ||||||
chr6:139276378
|
G | A | 37 | a0002c0002t0003g0240a0002c0009t0002g0167a0003c0003t0004g0064others(34): Show | 37 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.516+452C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276378 | ||||||
chr6:139276455
|
T | G | 1 | a0001c0004t0001g0010 | 2 | NA18964.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.516+375A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276455 | ||||||
chr6:139276457
|
C | T | 3 | a0005c0010t0013g0154a0005c0010t0013g0155a0009c0032t0028g0161 | 3 | HG02145.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.516+373G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276457 | ||||||
chr6:139276460
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0093 | 2 | HG01496.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.516+370C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276460 | ||||||
chr6:139276529
|
T | C | 20 | a0003c0003t0004g0064a0003c0003t0004g0080a0003c0003t0004g0112others(17): Show | 20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.516+301A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276529 | ||||||
chr6:139276654
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.516+176A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276654 | ||||||
chr6:139276697
|
G | A | 3 | a0003c0011t0005g0121a0004c0006t0005g0259a0004c0006t0005g0263 | 3 | HG02258.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.516+133C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276697 | ||||||
chr6:139276743
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.516+87C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276743 | ||||||
chr6:139276752
|
G | C | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+78C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276752 | ||||||
chr6:139276789
|
C | T | 1 | a0002c0002t0002g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.516+41G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276789 | ||||||
chr6:139276797
|
G | A | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+33C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276797 | ||||||
chr6:139276924
|
TA | T | 147 | a0001c0001t0001g0226a0001c0001t0024g0139a0001c0028t0001g0015others(144): Show | 157 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(154): Show |
splice_region_variant&intron_variant | LOW | c.425-4delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139276924 | ||||||
chr6:139277182
|
A | C | 72 | a0001c0001t0001g0226a0001c0001t0024g0139a0002c0002t0001g0190others(69): Show | 82 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.425-261T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277182 | ||||||
chr6:139277336
|
G | A | 1 | a0002c0002t0003g0225 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.425-415C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277336 | ||||||
chr6:139277412
|
G | A | 31 | a0002c0009t0005g0172a0003c0008t0001g0192a0003c0008t0002g0175others(28): Show | 31 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-491C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277412 | ||||||
chr6:139277434
|
T | A | 33 | a0002c0009t0005g0172a0003c0008t0001g0192a0003c0008t0002g0175others(30): Show | 33 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.425-513A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277434 | ||||||
chr6:139277455
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0072 | 2 | NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.425-534G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277455 | ||||||
chr6:139277548
|
T | G | 1 | a0004c0005t0002g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.425-627A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277548 | ||||||
chr6:139277723
|
TA | T | 27 | a0002c0009t0005g0172a0003c0008t0002g0245a0003c0008t0008g0111others(24): Show | 27 | HG01081.hp1 HG01106.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.425-803delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277723 | ||||||
chr6:139277816
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0137others(1): Show | 4 | HG01109.hp1 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-895A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277816 | ||||||
chr6:139277909
|
C | T | 1 | a0017c0020t0002g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425-988G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277909 | ||||||
chr6:139278072
|
C | T | 73 | a0001c0001t0001g0226a0001c0001t0024g0139a0002c0002t0001g0190others(70): Show | 83 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.425-1151G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278072 | ||||||
chr6:139278117
|
A | G | 49 | a0002c0002t0003g0240a0002c0009t0002g0167a0002c0009t0005g0172others(46): Show | 49 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.425-1196T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278117 | ||||||
chr6:139278193
|
A | T | 1 | a0001c0001t0015g0040 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.425-1272T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278193 | ||||||
chr6:139278194
|
T | C | 1 | a0004c0005t0002g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.425-1273A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278194 | ||||||
chr6:139278197
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.425-1276A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278197 | ||||||
chr6:139278335
|
A | G | 5 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151others(2): Show | 5 | HG00558.hp1 HG01243.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-1414T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278335 | ||||||
chr6:139278629
|
C | CTG | 64 | a0001c0028t0001g0015a0002c0002t0003g0240a0002c0009t0002g0167others(61): Show | 64 | HG00323.hp2 HG00558.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.425-1709_425-1708i others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278629 | ||||||
chr6:139278702
|
A | G | 1 | a0005c0010t0005g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-1781T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278702 | ||||||
chr6:139278713
|
A | G | 70 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0001g0131others(67): Show | 80 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.425-1792T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278713 | ||||||
chr6:139278732
|
A | G | 1 | a0003c0008t0001g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.425-1811T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278732 | ||||||
chr6:139278768
|
G | A | 2 | a0011c0022t0005g0014a0015c0024t0027g0130 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.425-1847C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278768 | ||||||
chr6:139278776
|
C | T | 1 | a0002c0030t0003g0243 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-1855G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278776 | ||||||
chr6:139278780
|
C | T | 10 | a0001c0001t0003g0117a0002c0002t0002g0013a0002c0002t0002g0246others(7): Show | 11 | HG01175.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.425-1859G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278780 | ||||||
chr6:139278781
|
G | A | 8 | a0003c0008t0008g0111a0003c0008t0026g0110a0003c0012t0005g0168others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-1860C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278781 | ||||||
chr6:139278787
|
C | T | 8 | a0003c0008t0008g0111a0003c0008t0026g0110a0003c0012t0005g0168others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-1866G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278787 | ||||||
chr6:139278816
|
C | T | 3 | a0001c0001t0001g0124a0001c0004t0001g0264a0007c0034t0001g0265 | 3 | HG01106.hp1 NA18973.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.425-1895G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278816 | ||||||
chr6:139278833
|
A | G | 3 | a0001c0001t0001g0076a0010c0021t0001g0020a0018c0019t0001g0253 | 3 | HG01261.hp1 HG02717.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.425-1912T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278833 | ||||||
chr6:139278873
|
A | G | 9 | a0001c0001t0001g0063a0001c0028t0001g0015a0002c0002t0003g0023others(6): Show | 9 | HG00558.hp1 HG00733.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-1952T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278873 | ||||||
chr6:139278884
|
G | A | 2 | a0002c0002t0003g0183a0002c0002t0003g0186 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.425-1963C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278884 | ||||||
chr6:139278990
|
G | A | 75 | a0001c0001t0001g0058a0001c0001t0001g0226a0001c0001t0001g0241others(72): Show | 84 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.425-2069C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278990 | ||||||
chr6:139279099
|
T | C | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.425-2178A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279099 | ||||||
chr6:139279190
|
T | C | 67 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0202others(64): Show | 76 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.425-2269A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279190 | ||||||
chr6:139279246
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.425-2325G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279246 | ||||||
chr6:139279280
|
G | A | 26 | a0002c0002t0003g0240a0002c0009t0002g0163a0002c0009t0002g0166others(23): Show | 26 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.425-2359C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279280 | ||||||
chr6:139279335
|
C | G | 75 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(72): Show | 84 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.425-2414G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279335 | ||||||
chr6:139279489
|
A | T | 22 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0004t0001g0003others(19): Show | 28 | HG00673.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.425-2568T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279489 | ||||||
chr6:139279513
|
T | A | 1 | a0003c0011t0018g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-2592A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279513 | ||||||
chr6:139279627
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.425-2706G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279627 | ||||||
chr6:139279743
|
C | CA | 31 | a0002c0009t0002g0163a0002c0009t0002g0166a0002c0009t0002g0167others(28): Show | 31 | HG01081.hp1 HG01106.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-2823dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279743 | ||||||
chr6:139279849
|
G | A | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.425-2928C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279849 | ||||||
chr6:139279878
|
T | G | 1 | a0003c0014t0008g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.425-2957A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279878 | ||||||
chr6:139279911
|
G | A | 1 | a0002c0002t0003g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.425-2990C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279911 | ||||||
chr6:139279978
|
A | G | 12 | a0003c0003t0004g0187a0003c0003t0004g0195a0003c0003t0004g0196others(9): Show | 12 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-3057T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279978 | ||||||
chr6:139279997
|
C | T | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.425-3076G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279997 | ||||||
chr6:139279999
|
A | G | 98 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0134others(95): Show | 113 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.425-3078T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279999 | ||||||
chr6:139280002
|
G | A | 2 | a0003c0008t0002g0175a0005c0010t0005g0181 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.425-3081C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280002 | ||||||
chr6:139280013
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.425-3092A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280013 | ||||||
chr6:139280068
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.425-3147G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280068 | ||||||
chr6:139280088
|
T | A | 132 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0134others(129): Show | 147 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.425-3167A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280088 | ||||||
chr6:139280251
|
TA | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 144 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.425-3331delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280251 | ||||||
chr6:139280266
|
A | G | 98 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0134others(95): Show | 113 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.425-3345T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280266 | ||||||
chr6:139280268
|
A | G | 2 | a0014c0027t0021g0244a0018c0019t0001g0253 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.425-3347T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280268 | ||||||
chr6:139280272
|
A | G | 34 | a0001c0028t0001g0015a0002c0009t0002g0166a0002c0009t0002g0167others(31): Show | 34 | HG00558.hp1 HG01081.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-3351T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280272 | ||||||
chr6:139280283
|
A | G | 3 | a0002c0002t0003g0159a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.425-3362T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280283 | ||||||
chr6:139280297
|
A | C | 1 | a0003c0011t0018g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-3376T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280297 | ||||||
chr6:139280471
|
G | A | 86 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(83): Show | 101 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.425-3550C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280471 | ||||||
chr6:139280495
|
A | T | 98 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(95): Show | 113 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.425-3574T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280495 | ||||||
chr6:139280505
|
C | A | 12 | a0001c0001t0001g0133a0002c0002t0003g0159a0003c0003t0004g0153others(9): Show | 12 | HG01109.hp2 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-3584G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280505 | ||||||
chr6:139280547
|
A | AG | 98 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(95): Show | 113 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.425-3627dupC | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280547 | ||||||
chr6:139280676
|
A | AT | 92 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(89): Show | 107 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.425-3756dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280676 | ||||||
chr6:139280719
|
G | A | 97 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(94): Show | 112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-3798C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280719 | ||||||
chr6:139281041
|
GATTTATT others(1): Show |
G | 6 | a0003c0011t0018g0152a0005c0010t0013g0154a0005c0010t0013g0155others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-4128_425-4121d others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281041 | ||||||
chr6:139281058
|
T | A | 24 | a0001c0001t0001g0133a0001c0001t0001g0241a0002c0002t0002g0013others(21): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.425-4137A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281058 | ||||||
chr6:139281066
|
T | A | 2 | a0003c0008t0002g0175a0005c0010t0005g0181 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.425-4145A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281066 | ||||||
chr6:139281084
|
G | T | 2 | a0002c0030t0003g0243a0003c0031t0022g0242 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.425-4163C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281084 | ||||||
chr6:139281180
|
T | C | 97 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(94): Show | 112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-4259A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281180 | ||||||
chr6:139281198
|
A | T | 97 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(94): Show | 112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-4277T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281198 | ||||||
chr6:139281251
|
C | T | 1 | a0001c0001t0029g0061 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-4330G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281251 | ||||||
chr6:139281302
|
T | A | 141 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0134others(138): Show | 157 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.425-4381A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281302 | ||||||
chr6:139281330
|
C | T | 97 | a0001c0001t0001g0036a0001c0001t0001g0134a0001c0001t0001g0135others(94): Show | 112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-4409G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281330 | ||||||
chr6:139281398
|
G | A | 2 | a0002c0030t0003g0243a0003c0031t0022g0242 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.425-4477C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281398 | ||||||
chr6:139281461
|
CTCTTATC others(4543): Show |
C | 64 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(61): Show | 71 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.424+2465_425-4541d others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281461 | ||||||
chr6:139281495
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | NA18960.hp2 NA18995.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-4574C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281495 | ||||||
chr6:139281530
|
TCTGGAGT others(310): Show |
T | 79 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(76): Show | 88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.425-4926_425-4610d others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281530 | ||||||
chr6:139281538
|
T | TC | 7 | a0001c0001t0001g0056a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 7 | HG01255.hp2 NA18959.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-4618dupG | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281538 | ||||||
chr6:139281539
|
C | CT | 33 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 34 | HG00597.hp2 HG00738.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-4619dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281539 | ||||||
chr6:139281611
|
C | G | 1 | a0001c0001t0029g0061 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-4690G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281611 | ||||||
chr6:139281999
|
C | T | 3 | a0002c0002t0003g0159a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.425-5078G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281999 | ||||||
chr6:139282053
|
T | G | 27 | a0003c0003t0004g0112a0003c0003t0004g0148a0003c0003t0016g0149others(24): Show | 27 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.425-5132A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282053 | ||||||
chr6:139282120
|
T | C | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5199A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282120 | ||||||
chr6:139282256
|
A | G | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5335T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282256 | ||||||
chr6:139282272
|
G | A | 6 | a0003c0011t0018g0152a0005c0010t0013g0154a0005c0010t0013g0155others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-5351C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282272 | ||||||
chr6:139282277
|
G | A | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5356C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282277 | ||||||
chr6:139282305
|
G | A | 1 | a0002c0002t0007g0113 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.425-5384C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282305 | ||||||
chr6:139282335
|
G | A | 22 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(19): Show | 28 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.425-5414C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282335 | ||||||
chr6:139282337
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.425-5416C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282337 | ||||||
chr6:139282502
|
G | A | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5581C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282502 | ||||||
chr6:139282607
|
G | A | 13 | a0002c0002t0002g0013a0002c0002t0002g0246a0002c0002t0002g0248others(10): Show | 14 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.425-5686C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282607 | ||||||
chr6:139282766
|
G | A | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+5710C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282766 | ||||||
chr6:139282787
|
A | C | 10 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151others(7): Show | 10 | HG00558.hp1 HG01891.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5689T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282787 | ||||||
chr6:139282996
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.424+5480T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282996 | ||||||
chr6:139283065
|
C | T | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+5411G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283065 | ||||||
chr6:139283178
|
G | A | 2 | a0008c0015t0011g0254a0008c0015t0011g0255 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.424+5298C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283178 | ||||||
chr6:139283271
|
T | TA | 8 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0057others(5): Show | 8 | HG00639.hp2 HG00738.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+5204dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | ||||||
chr6:139283271
|
TA | T | 33 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(30): Show | 40 | HG00673.hp1 HG01109.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.424+5204delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | ||||||
chr6:139283271
|
TAA | T | 23 | a0001c0001t0001g0133a0001c0028t0001g0015a0002c0002t0002g0182others(20): Show | 25 | HG00558.hp1 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+5203_424+5204d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | ||||||
chr6:139283345
|
C | G | 79 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(76): Show | 88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+5131G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283345 | ||||||
chr6:139283367
|
G | A | 1 | a0017c0020t0002g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+5109C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283367 | ||||||
chr6:139283490
|
C | T | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4986G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283490 | ||||||
chr6:139283525
|
G | A | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4951C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283525 | ||||||
chr6:139283528
|
A | T | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+4948T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283528 | ||||||
chr6:139283563
|
C | T | 17 | a0001c0001t0001g0133a0002c0002t0002g0013a0002c0002t0002g0246others(14): Show | 18 | HG01109.hp2 HG02135.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.424+4913G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283563 | ||||||
chr6:139283576
|
C | CA | 28 | a0001c0001t0001g0060a0001c0001t0001g0120a0001c0001t0001g0132others(25): Show | 34 | HG00673.hp1 HG01261.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+4899dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283576 | ||||||
chr6:139283576
|
CA | C | 24 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(21): Show | 25 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+4899delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283576 | ||||||
chr6:139283848
|
A | G | 8 | a0002c0002t0002g0182a0002c0002t0002g0184a0002c0002t0003g0004others(5): Show | 10 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4628T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283848 | ||||||
chr6:139283967
|
A | C | 2 | a0001c0001t0001g0060a0002c0002t0003g0059 | 2 | HG01943.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.424+4509T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283967 | ||||||
chr6:139284098
|
C | G | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4378G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284098 | ||||||
chr6:139284119
|
A | G | 4 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151others(1): Show | 4 | HG00558.hp1 HG01891.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4357T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284119 | ||||||
chr6:139284142
|
C | T | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4334G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284142 | ||||||
chr6:139284267
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4209G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284267 | ||||||
chr6:139284444
|
C | T | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4032G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284444 | ||||||
chr6:139284459
|
T | A | 1 | a0001c0004t0001g0268 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.424+4017A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284459 | ||||||
chr6:139284485
|
G | A | 2 | a0004c0005t0002g0141a0004c0005t0002g0146 | 2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.424+3991C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284485 | ||||||
chr6:139284579
|
G | T | 79 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(76): Show | 88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+3897C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284579 | ||||||
chr6:139284643
|
C | A | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3833G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284643 | ||||||
chr6:139284762
|
C | A | 8 | a0004c0006t0005g0256a0004c0006t0005g0258a0004c0006t0005g0259others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+3714G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284762 | ||||||
chr6:139284777
|
G | A | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.424+3699C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284777 | ||||||
chr6:139284814
|
A | G | 1 | a0004c0006t0005g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.424+3662T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284814 | ||||||
chr6:139284840
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+3636G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284840 | ||||||
chr6:139284922
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.424+3554T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284922 | ||||||
chr6:139285010
|
T | C | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3466A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285010 | ||||||
chr6:139285036
|
G | A | 81 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(78): Show | 90 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.424+3440C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285036 | ||||||
chr6:139285093
|
C | T | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3383G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285093 | ||||||
chr6:139285094
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+3382C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285094 | ||||||
chr6:139285246
|
T | A | 1 | a0004c0005t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.424+3230A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285246 | ||||||
chr6:139285257
|
A | AAC | 10 | a0001c0001t0001g0029a0001c0001t0001g0132a0002c0002t0002g0246others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+3217_424+3218d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
A | AACAC | 3 | a0003c0008t0002g0245a0004c0006t0005g0258a0004c0017t0005g0257 | 3 | HG02486.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.424+3215_424+3218d others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
A | AACACAC | 4 | a0002c0002t0003g0159a0004c0006t0005g0256a0005c0013t0010g0158others(1): Show | 4 | HG02109.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+3213_424+3218d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AAC | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0035others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+3217_424+3218d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACAC | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0043others(32): Show | 36 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.424+3215_424+3218d others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACACAC | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 90 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.424+3213_424+3218d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACACACA others(1): Show |
A | 14 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(11): Show | 16 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+3211_424+3218d others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACACACA others(3): Show |
A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0002c0002t0002g0182others(2): Show | 5 | HG01884.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+3209_424+3218d others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACACACA others(5): Show |
A | 19 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0264others(16): Show | 24 | HG00673.hp1 HG02040.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+3207_424+3218d others(14): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285257
|
AACACACA others(7): Show |
A | 3 | a0001c0001t0001g0133a0001c0004t0001g0010a0002c0009t0002g0174 | 4 | HG02647.hp1 HG02970.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+3205_424+3218d others(16): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | ||||||
chr6:139285416
|
C | T | 19 | a0004c0005t0002g0141a0004c0005t0002g0142a0004c0005t0002g0143others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+3060G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285416 | ||||||
chr6:139285594
|
T | C | 59 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(56): Show | 68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+2882A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285594 | ||||||
chr6:139285706
|
C | G | 1 | a0017c0020t0002g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+2770G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285706 | ||||||
chr6:139285717
|
G | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+2759C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285717 | ||||||
chr6:139285809
|
C | G | 1 | a0018c0019t0001g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+2667G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285809 | ||||||
chr6:139285818
|
C | T | 2 | a0003c0003t0004g0148a0003c0003t0016g0149 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.424+2658G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285818 | ||||||
chr6:139285833
|
C | A | 1 | a0014c0027t0021g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+2643G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285833 | ||||||
chr6:139285927
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0002c0002t0003g0026others(2): Show | 5 | HG00323.hp1 HG01975.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2549G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285927 | ||||||
chr6:139285947
|
C | T | 19 | a0004c0005t0002g0141a0004c0005t0002g0142a0004c0005t0002g0143others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+2529G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285947 | ||||||
chr6:139285999
|
T | G | 79 | a0001c0001t0001g0133a0001c0004t0001g0003a0001c0004t0001g0005others(76): Show | 88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+2477A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285999 | ||||||
chr6:139286011
|
T | C | 15 | a0002c0002t0002g0184a0002c0002t0003g0004a0002c0002t0003g0183others(12): Show | 17 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+2465A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286011 | ||||||
chr6:139286201
|
G | C | 1 | a0002c0025t0003g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+2275C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286201 | ||||||
chr6:139286225
|
T | C | 123 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(120): Show | 139 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.424+2251A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286225 | ||||||
chr6:139286264
|
C | G | 1 | a0003c0031t0022g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+2212G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286264 | ||||||
chr6:139286328
|
C | T | 5 | a0006c0007t0002g0178a0006c0007t0002g0179a0006c0007t0005g0176others(2): Show | 5 | HG02572.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2148G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286328 | ||||||
chr6:139286353
|
T | C | 112 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(109): Show | 128 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.424+2123A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286353 | ||||||
chr6:139286438
|
A | G | 2 | a0002c0002t0001g0190a0002c0002t0001g0191 | 2 | NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.424+2038T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286438 | ||||||
chr6:139286489
|
A | G | 120 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(117): Show | 136 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.424+1987T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286489 | ||||||
chr6:139286504
|
C | T | 1 | a0002c0002t0003g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.424+1972G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286504 | ||||||
chr6:139286510
|
G | A | 120 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(117): Show | 136 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.424+1966C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286510 | ||||||
chr6:139286538
|
A | G | 121 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0134others(118): Show | 137 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.424+1938T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286538 | ||||||
chr6:139286588
|
C | A | 64 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(61): Show | 71 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.424+1888G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286588 | ||||||
chr6:139286635
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.424+1841G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286635 | ||||||
chr6:139286636
|
G | A | 22 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(19): Show | 28 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+1840C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286636 | ||||||
chr6:139286685
|
T | C | 62 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(59): Show | 69 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.424+1791A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286685 | ||||||
chr6:139286768
|
T | A | 1 | a0017c0020t0002g0252 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+1708A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286768 | ||||||
chr6:139286861
|
A | G | 120 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(117): Show | 136 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.424+1615T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286861 | ||||||
chr6:139286932
|
T | C | 3 | a0002c0002t0003g0159a0005c0013t0010g0158a0005c0013t0010g0160 | 3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.424+1544A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286932 | ||||||
chr6:139286992
|
G | A | 33 | a0001c0001t0001g0133a0002c0002t0002g0013a0002c0002t0002g0246others(30): Show | 34 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+1484C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286992 | ||||||
chr6:139287029
|
C | T | 32 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(29): Show | 40 | HG00673.hp1 HG00735.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.424+1447G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287029 | ||||||
chr6:139287050
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+1426G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287050 | ||||||
chr6:139287742
|
T | C | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+734A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287742 | ||||||
chr6:139287834
|
G | A | 8 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151others(5): Show | 8 | HG00558.hp1 HG02071.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+642C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287834 | ||||||
chr6:139287875
|
G | GT | 120 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(117): Show | 136 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.424+600dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287875 | ||||||
chr6:139287916
|
T | C | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.424+560A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287916 | ||||||
chr6:139288087
|
A | C | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.424+389T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139288087 | ||||||
chr6:139288258
|
G | A | 20 | a0004c0005t0002g0141a0004c0005t0002g0142a0004c0005t0002g0143others(17): Show | 20 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+218C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139288258 | ||||||
chr6:139288932
|
AGGCTTTA others(43): Show |
A | 1 | a0004c0005t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-69_-14-20delCA others(48): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139288932 | ||||||
chr6:139288987
|
G | T | 73 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(70): Show | 82 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-14-74C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139288987 | ||||||
chr6:139289032
|
GAGAA | G | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-14-123_-14-120del others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289032 | ||||||
chr6:139289039
|
G | T | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-14-126C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289039 | ||||||
chr6:139289040
|
C | G | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-14-127G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289040 | ||||||
chr6:139289334
|
CT | C | 73 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(70): Show | 82 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-14-422delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289334 | ||||||
chr6:139289462
|
C | T | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-549G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289462 | ||||||
chr6:139289525
|
G | A | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-14-612C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289525 | ||||||
chr6:139289537
|
T | G | 129 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(126): Show | 145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-14-624A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289537 | ||||||
chr6:139289561
|
G | GT | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(18): Show | 27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-14-649dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289561 | ||||||
chr6:139289791
|
A | C | 129 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(126): Show | 145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-14-878T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289791 | ||||||
chr6:139289811
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-14-898A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289811 | ||||||
chr6:139289859
|
A | G | 143 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(140): Show | 159 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-14-946T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289859 | ||||||
chr6:139289966
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-1053A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289966 | ||||||
chr6:139290211
|
C | T | 130 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(127): Show | 146 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-14-1298G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290211 | ||||||
chr6:139290255
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0017c0020t0002g0252 | 3 | HG02109.hp2 NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-14-1342G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290255 | ||||||
chr6:139290317
|
C | T | 130 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(127): Show | 146 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-14-1404G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290317 | ||||||
chr6:139290337
|
G | GCCCCCCC others(40): Show |
1 | a0004c0005t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1425_-14-1424i others(49): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290337 | ||||||
chr6:139290340
|
A | G | 1 | a0004c0005t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1427T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290340 | ||||||
chr6:139290342
|
T | C | 1 | a0004c0005t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1429A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290342 | ||||||
chr6:139290343
|
G | C | 1 | a0004c0005t0002g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1430C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290343 | ||||||
chr6:139290482
|
G | C | 7 | a0002c0002t0002g0013a0002c0002t0002g0246a0002c0002t0002g0248others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1439C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290482 | ||||||
chr6:139290500
|
T | A | 1 | a0002c0025t0003g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-15+1421A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290500 | ||||||
chr6:139290552
|
G | T | 1 | a0003c0008t0002g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+1369C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290552 | ||||||
chr6:139290554
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | NA18939.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-15+1367T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290554 | ||||||
chr6:139290562
|
A | G | 13 | a0001c0028t0001g0015a0002c0002t0003g0159a0002c0016t0006g0150others(10): Show | 13 | HG00558.hp1 HG01109.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+1359T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290562 | ||||||
chr6:139290606
|
A | G | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(18): Show | 27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+1315T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290606 | ||||||
chr6:139290618
|
G | A | 110 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(107): Show | 126 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+1303C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290618 | ||||||
chr6:139290625
|
T | A | 20 | a0004c0005t0002g0141a0004c0005t0002g0142a0004c0005t0002g0143others(17): Show | 20 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+1296A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290625 | ||||||
chr6:139290633
|
G | A | 8 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0010others(5): Show | 14 | HG00673.hp1 HG02040.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+1288C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290633 | ||||||
chr6:139290669
|
A | C | 1 | a0001c0004t0001g0010 | 2 | NA18964.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-15+1252T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290669 | ||||||
chr6:139290906
|
A | G | 130 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(127): Show | 146 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-15+1015T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290906 | ||||||
chr6:139291130
|
C | G | 3 | a0001c0028t0001g0015a0002c0016t0006g0150a0002c0016t0006g0151 | 3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-15+791G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291130 | ||||||
chr6:139291184
|
G | C | 1 | a0002c0002t0003g0269 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-15+737C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291184 | ||||||
chr6:139291231
|
C | T | 1 | a0011c0022t0005g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-15+690G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291231 | ||||||
chr6:139291275
|
G | C | 130 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(127): Show | 146 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-15+646C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291275 | ||||||
chr6:139291317
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-15+604A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291317 | ||||||
chr6:139291334
|
A | G | 2 | a0003c0003t0004g0148a0003c0003t0016g0149 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+587T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291334 | ||||||
chr6:139291801
|
A | G | 8 | a0004c0005t0002g0141a0004c0005t0002g0142a0004c0005t0002g0143others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+120T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291801 | ||||||
chr6:139291871
|
C | T | 1 | a0001c0001t0024g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-15+50G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291871 | ||||||
chr6:139291880
|
T | C | 140 | a0001c0001t0001g0202a0001c0001t0001g0226a0001c0001t0001g0241others(137): Show | 156 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.-15+41A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291880 |