Item | Value |
---|---|
geneid | 7148 |
ensemblid | ENSG00000168477.21 |
hgncid | 11976 |
symbol | TNXB |
name | tenascin XB |
refseq_nuc | NM_001365276.2 |
refseq_prot | NP_001352205.1 |
ensembl_nuc | ENST00000644971.2 |
ensembl_prot | ENSP00000496448.1 |
mane_status | MANE Select |
chr | chr6 |
start | 32041153 |
end | 32109338 |
strand | - |
ver | v1.2 |
region | chr6:32041153-32109338 |
region5000 | chr6:32036153-32114338 |
regionname0 | TNXB_chr6_32041153_32109338 |
regionname5000 | TNXB_chr6_32036153_32114338 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 4244 | 62 | 1 | 18 | 36 | 3 | 4 | 32 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0002 | 0/0 | 4244 | 47 | 4 | 11 | 29 | 0 | 3 | 24 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0003 | 0/0 | 4244 | 22 | 0 | 0 | 22 | 0 | 0 | 14 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0004 | 0/0 | 4244 | 20 | 11 | 4 | 4 | 0 | 1 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0005 | 0/0 | 4244 | 17 | 0 | 1 | 16 | 0 | 0 | 14 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0006 | 0/0 | 4244 | 14 | 6 | 0 | 2 | 2 | 4 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0007 | 0/0 | 4244 | 14 | 8 | 6 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0008 | 0/0 | 4244 | 14 | 1 | 0 | 13 | 0 | 0 | 13 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0009 | 0/0 | 4244 | 11 | 6 | 0 | 5 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0010 | 0/0 | 4244 | 11 | 5 | 4 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0011 | 0/0 | 4244 | 10 | 2 | 4 | 1 | 1 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0012 | 0/0 | 4244 | 7 | 4 | 0 | 2 | 0 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0013 | 0/0 | 4244 | 6 | 0 | 3 | 2 | 1 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0014 | 0/0 | 4244 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0015 | 0/0 | 4244 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0016 | 0/0 | 4244 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0017 | 0/0 | 4244 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0018 | 0/0 | 4244 | 5 | 1 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0019 | 0/0 | 4133 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4128): Show |
chr6 | 32036153 | 32114338 |
a0020 | 0/0 | 4244 | 5 | 0 | 0 | 2 | 0 | 3 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0021 | 0/0 | 4244 | 4 | 1 | 0 | 3 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0022 | 0/0 | 4244 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0023 | 0/0 | 4244 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0024 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0025 | 0/0 | 4244 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0026 | 0/0 | 4244 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0027 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0028 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0029 | 0/0 | 4244 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0030 | 0/0 | 4244 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0031 | 0/0 | 4244 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0032 | 0/0 | 4244 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0033 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0034 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0035 | 0/0 | 4244 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0036 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0037 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0038 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0039 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0040 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0041 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0042 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0043 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0044 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0045 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0046 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0047 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0048 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0049 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0050 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0051 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0052 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0053 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0054 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0055 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0056 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0057 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0058 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0059 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0060 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0061 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0062 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0063 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0064 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0065 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0066 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0067 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0068 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0069 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0070 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0071 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0072 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0073 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0074 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0075 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0076 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0077 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0078 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0079 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0080 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(1675): Show |
chr6 | 32036153 | 32114338 |
a0081 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0082 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4209): Show |
chr6 | 32036153 | 32114338 |
a0083 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0084 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0085 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0086 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4244): Show |
chr6 | 32036153 | 32114338 |
a0087 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0088 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0089 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0090 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0091 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0092 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0093 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0094 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0095 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0096 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
a0097 | 0/1 | 4244 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | MMPAQ others(4239): Show |
chr6 | 32036153 | 32114338 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 12732 | 45 | 0 | 14 | 26 | 2 | 3 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0001c0007 | 0/0 | 12732 | 12 | 0 | 3 | 8 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0001c0034 | 0/0 | 12732 | 3 | 1 | 1 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0001c0109 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0001c0110 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0002 | 0/0 | 12732 | 27 | 0 | 2 | 22 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0012 | 0/0 | 12732 | 8 | 0 | 3 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0019 | 0/0 | 12732 | 5 | 0 | 5 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0040 | 0/0 | 12732 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0042 | 0/0 | 12732 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0093 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0095 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0002c0096 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0003c0003 | 0/0 | 12732 | 19 | 0 | 0 | 19 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0003c0048 | 0/0 | 12732 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0003c0113 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0004c0008 | 0/0 | 12732 | 10 | 8 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0004c0011 | 0/0 | 12732 | 9 | 2 | 2 | 4 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0004c0061 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0005c0013 | 0/0 | 12732 | 7 | 0 | 0 | 7 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0005c0023 | 0/0 | 12732 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0005c0024 | 0/0 | 12732 | 5 | 0 | 1 | 4 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0006c0006 | 0/0 | 12732 | 12 | 5 | 0 | 2 | 1 | 4 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0006c0045 | 0/0 | 12732 | 2 | 1 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0007c0004 | 0/0 | 12732 | 14 | 8 | 6 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0008c0005 | 0/0 | 12732 | 14 | 1 | 0 | 13 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0009c0020 | 0/0 | 12732 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0009c0029 | 0/0 | 12732 | 4 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0009c0069 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0009c0091 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0010c0010 | 0/0 | 12732 | 10 | 4 | 4 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0010c0087 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0011c0009 | 0/0 | 12732 | 10 | 2 | 4 | 1 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0012c0015 | 0/0 | 12732 | 6 | 3 | 0 | 2 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0012c0098 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0013c0018 | 0/0 | 12732 | 5 | 0 | 3 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0013c0080 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0014c0016 | 0/0 | 12732 | 6 | 0 | 0 | 6 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0015c0014 | 0/0 | 12732 | 6 | 0 | 1 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0016c0025 | 0/0 | 12732 | 5 | 0 | 3 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0017c0017 | 0/0 | 12732 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0018c0021 | 0/0 | 12732 | 5 | 1 | 4 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0019c0022 | 0/0 | 12399 | 5 | 5 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12394): Show |
chr6 | 32036153 | 32114338 | ||
a0020c0026 | 0/0 | 12732 | 4 | 0 | 0 | 1 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0020c0058 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0021c0027 | 0/0 | 12732 | 4 | 1 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0022c0028 | 0/0 | 12732 | 4 | 0 | 0 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0023c0032 | 0/0 | 12732 | 3 | 0 | 2 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0024c0052 | 0/0 | 12732 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0024c0125 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0025c0033 | 0/0 | 12732 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0026c0036 | 0/0 | 12732 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0026c0053 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0027c0035 | 0/0 | 12732 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0028c0037 | 0/0 | 12732 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0028c0068 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0029c0031 | 0/0 | 12732 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0030c0030 | 0/0 | 12732 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0031c0051 | 0/0 | 12732 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0032c0050 | 0/0 | 12732 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0033c0049 | 0/0 | 12732 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0034c0044 | 0/0 | 12732 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0035c0043 | 0/0 | 12732 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0036c0046 | 0/0 | 12732 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0037c0041 | 0/0 | 12732 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0038c0047 | 0/0 | 12732 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0039c0038 | 0/0 | 12732 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0040c0039 | 0/0 | 12732 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0041c0071 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0042c0070 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0043c0120 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0044c0089 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0045c0088 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0046c0066 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0047c0094 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0048c0075 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0049c0055 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0050c0102 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0051c0104 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0052c0116 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0053c0118 | 0/0 | 12732 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0054c0083 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0055c0111 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0056c0054 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0057c0122 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0058c0105 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0059c0078 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0060c0077 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0061c0076 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0062c0117 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0063c0099 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0064c0074 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0065c0085 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0066c0057 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0067c0060 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0068c0097 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0069c0065 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0070c0079 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0071c0115 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0072c0114 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0073c0123 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0074c0082 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0075c0056 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0076c0064 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0077c0107 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0078c0106 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0079c0081 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0080c0101 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0081c0062 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0082c0108 | 0/0 | 12642 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12637): Show |
chr6 | 32036153 | 32114338 | ||
a0083c0112 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0084c0086 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0085c0059 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0086c0084 | 0/0 | 12747 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12742): Show |
chr6 | 32036153 | 32114338 | ||
a0087c0124 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0088c0072 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0089c0090 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0090c0073 | 0/0 | 12732 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0091c0067 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0092c0121 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0093c0119 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0094c0100 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0095c0092 | 0/0 | 12732 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0096c0063 | 0/0 | 12732 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 | ||
a0097c0103 | 0/1 | 12732 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | ATGAT others(12727): Show |
chr6 | 32036153 | 32114338 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13097 | 44 | 0 | 14 | 26 | 1 | 3 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0001c0001t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0001c0007t0001 | 0/0 | 13097 | 12 | 0 | 3 | 8 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0001c0034t0001 | 0/0 | 13097 | 3 | 1 | 1 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0001c0109t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0001c0110t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0002t0001 | 0/0 | 13097 | 27 | 0 | 2 | 22 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0012t0002 | 0/0 | 13097 | 8 | 0 | 3 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0019t0002 | 0/0 | 13097 | 5 | 0 | 5 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0040t0002 | 0/0 | 13097 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0042t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0093t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0095t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0002c0096t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0003c0003t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0003c0003t0002 | 0/0 | 13097 | 18 | 0 | 0 | 18 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0003c0048t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0003c0048t0005 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0003c0113t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0004c0008t0001 | 0/0 | 13097 | 10 | 8 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0004c0011t0001 | 0/0 | 13097 | 9 | 2 | 2 | 4 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0004c0061t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0005c0013t0001 | 0/0 | 13097 | 7 | 0 | 0 | 7 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0005c0023t0001 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0005c0024t0001 | 0/0 | 13097 | 5 | 0 | 1 | 4 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0006c0006t0001 | 0/0 | 13097 | 12 | 5 | 0 | 2 | 1 | 4 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0006c0045t0001 | 0/0 | 13097 | 2 | 1 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0007c0004t0001 | 0/0 | 13097 | 14 | 8 | 6 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0008c0005t0002 | 0/0 | 13097 | 14 | 1 | 0 | 13 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0009c0020t0001 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0009c0029t0001 | 0/0 | 13097 | 4 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0009c0069t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0009c0091t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0010c0010t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0010c0010t0002 | 0/0 | 13097 | 9 | 3 | 4 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0010c0087t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0011c0009t0002 | 0/0 | 13097 | 10 | 2 | 4 | 1 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0012c0015t0001 | 0/0 | 13097 | 6 | 3 | 0 | 2 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0012c0098t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0013c0018t0002 | 0/0 | 13097 | 5 | 0 | 3 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0013c0080t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0014c0016t0002 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0014c0016t0006 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0015c0014t0001 | 0/0 | 13097 | 6 | 0 | 1 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0016c0025t0002 | 0/0 | 13097 | 5 | 0 | 3 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0017c0017t0003 | 0/0 | 13097 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0018c0021t0002 | 0/0 | 13097 | 5 | 1 | 4 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0019c0022t0002 | 0/0 | 12764 | 5 | 5 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(12759): Show |
chr6 | 32036153 | 32114338 |
a0020c0026t0001 | 0/0 | 13097 | 4 | 0 | 0 | 1 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0020c0058t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0021c0027t0001 | 0/0 | 13097 | 4 | 1 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0022c0028t0002 | 0/0 | 13097 | 4 | 0 | 0 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0023c0032t0001 | 0/0 | 13097 | 3 | 0 | 2 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0024c0052t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0024c0125t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0025c0033t0002 | 0/0 | 13097 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0026c0036t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0026c0053t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0027c0035t0001 | 0/0 | 13097 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0028c0037t0001 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0028c0068t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0029c0031t0001 | 0/0 | 13097 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0030c0030t0001 | 0/0 | 13097 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0031c0051t0001 | 0/0 | 13097 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0032c0050t0002 | 0/0 | 13097 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0033c0049t0002 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0034c0044t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0035c0043t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0036c0046t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0037c0041t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0038c0047t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0039c0038t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0040c0039t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0041c0071t0007 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0042c0070t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0043c0120t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0044c0089t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0045c0088t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0046c0066t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0047c0094t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0048c0075t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0049c0055t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0050c0102t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0051c0104t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0052c0116t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0053c0118t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0054c0083t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0055c0111t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0056c0054t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0057c0122t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0058c0105t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0059c0078t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0060c0077t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0061c0076t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0062c0117t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0063c0099t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0064c0074t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0065c0085t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0066c0057t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0067c0060t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0068c0097t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0069c0065t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0070c0079t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0071c0115t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0072c0114t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0073c0123t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0074c0082t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0075c0056t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0076c0064t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0077c0107t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0078c0106t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0079c0081t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0080c0101t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0081c0062t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0082c0108t0002 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13002): Show |
chr6 | 32036153 | 32114338 |
a0083c0112t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0084c0086t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0085c0059t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0086c0084t0001 | 0/0 | 13112 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13107): Show |
chr6 | 32036153 | 32114338 |
a0087c0124t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0088c0072t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0089c0090t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0090c0073t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0091c0067t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0092c0121t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0093c0119t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0094c0100t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0095c0092t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0096c0063t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
a0097c0103t0001 | 0/1 | 13097 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | CTCCT others(13092): Show |
chr6 | 32036153 | 32114338 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0109t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0110t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0040t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0040t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0042t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0042t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0093t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0095t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0096t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0048t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0048t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0113t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0061t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0006t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0045t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0045t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0001 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0005t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0029t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0029t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0029t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0029t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0069t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0091t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0087t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0098t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0018t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0018t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0018t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0018t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0080t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0016t0006g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0014t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0025t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0025t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0025t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0025t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0025t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0017t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0017t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0017t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0017t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0017t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0022t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0022t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0022t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0022t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0022t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0026t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0026t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0026t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0026t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0058t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0027t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0027t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0028t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0028t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0028t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0028t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0023c0032t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0023c0032t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0023c0032t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0024c0052t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0024c0125t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0025c0033t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0025c0033t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0025c0033t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0026c0036t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0026c0053t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0027c0035t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0027c0035t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0027c0035t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0028c0037t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0028c0068t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0031t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0031t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0031t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0030t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0030t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0030t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0031c0051t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0031c0051t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0032c0050t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0032c0050t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0033c0049t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0033c0049t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0034c0044t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0035c0043t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0035c0043t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0036c0046t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0036c0046t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0037c0041t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0037c0041t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0038c0047t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0038c0047t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0039c0038t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0039c0038t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0040c0039t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0040c0039t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0041c0071t0007g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0042c0070t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0043c0120t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0044c0089t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0045c0088t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0046c0066t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0047c0094t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0048c0075t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0049c0055t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0050c0102t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0051c0104t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0052c0116t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0053c0118t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0054c0083t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0055c0111t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0056c0054t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0057c0122t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0058c0105t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0059c0078t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0060c0077t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0061c0076t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0062c0117t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0063c0099t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0064c0074t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0065c0085t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0066c0057t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0067c0060t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0068c0097t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0069c0065t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0070c0079t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0071c0115t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0072c0114t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0073c0123t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0074c0082t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0075c0056t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0076c0064t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0077c0107t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0078c0106t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0079c0081t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0080c0101t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0081c0062t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0082c0108t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0083c0112t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0084c0086t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0085c0059t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0086c0084t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0087c0124t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0088c0072t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0089c0090t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0090c0073t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0091c0067t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0092c0121t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0093c0119t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0094c0100t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0095c0092t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0096c0063t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0097c0103t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0016 | c0025 | t0002 | g0089 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00140 | hp1 | a0006 | c0006 | t0001 | g0317 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00140 | hp2 | a0041 | c0071 | t0007 | g0373 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00280 | hp1 | a0016 | c0025 | t0002 | g0088 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00323 | hp1 | a0013 | c0080 | t0002 | g0084 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00323 | hp2 | a0042 | c0070 | t0002 | g0201 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00408 | hp1 | a0002 | c0012 | t0002 | g0043 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00408 | hp2 | a0014 | c0016 | t0002 | g0351 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00423 | hp1 | a0003 | c0003 | t0002 | g0345 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00423 | hp2 | a0009 | c0020 | t0001 | g0051 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00438 | hp1 | a0043 | c0120 | t0002 | g0238 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00438 | hp2 | a0003 | c0003 | t0002 | g0354 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00558 | hp1 | a0004 | c0011 | t0001 | g0183 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0357 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00597 | hp1 | a0002 | c0012 | t0002 | g0041 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00597 | hp2 | a0009 | c0020 | t0001 | g0077 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00609 | hp1 | a0001 | c0034 | t0001 | g0254 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00609 | hp2 | a0014 | c0016 | t0002 | g0350 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00639 | hp1 | a0001 | c0007 | t0001 | g0272 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00642 | hp1 | a0031 | c0051 | t0001 | g0030 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00642 | hp2 | a0011 | c0009 | t0002 | g0002 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00673 | hp1 | a0044 | c0089 | t0001 | g0136 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00673 | hp2 | a0045 | c0088 | t0001 | g0023 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00733 | hp1 | a0001 | c0007 | t0001 | g0275 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00733 | hp2 | a0011 | c0009 | t0002 | g0050 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00735 | hp1 | a0032 | c0050 | t0002 | g0027 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00735 | hp2 | a0002 | c0019 | t0002 | g0065 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00738 | hp1 | a0016 | c0025 | t0002 | g0052 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00738 | hp2 | a0017 | c0017 | t0003 | g0205 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00741 | hp1 | a0002 | c0040 | t0002 | g0094 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00741 | hp2 | a0004 | c0008 | t0001 | g0191 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01069 | hp1 | a0016 | c0025 | t0002 | g0090 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01069 | hp2 | a0007 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01070 | hp1 | a0023 | c0032 | t0001 | g0180 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01070 | hp2 | a0016 | c0025 | t0002 | g0087 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01071 | hp1 | a0007 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01071 | hp2 | a0023 | c0032 | t0001 | g0189 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01074 | hp1 | a0010 | c0010 | t0002 | g0029 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01081 | hp1 | a0031 | c0051 | t0001 | g0031 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01099 | hp1 | a0007 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01099 | hp2 | a0010 | c0010 | t0002 | g0033 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01109 | hp1 | a0010 | c0010 | t0002 | g0034 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01167 | hp1 | a0018 | c0021 | t0002 | g0251 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01167 | hp2 | a0007 | c0004 | t0001 | g0197 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01169 | hp1 | a0007 | c0004 | t0001 | g0195 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01169 | hp2 | a0001 | c0034 | t0001 | g0262 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01175 | hp2 | a0004 | c0008 | t0001 | g0014 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01192 | hp1 | a0018 | c0021 | t0002 | g0248 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01243 | hp1 | a0046 | c0066 | t0001 | g0210 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01243 | hp2 | a0017 | c0017 | t0003 | g0209 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01255 | hp1 | a0002 | c0019 | t0002 | g0003 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01256 | hp1 | a0002 | c0019 | t0002 | g0003 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01256 | hp2 | a0013 | c0018 | t0002 | g0010 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01257 | hp1 | a0004 | c0011 | t0001 | g0182 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01257 | hp2 | a0011 | c0009 | t0002 | g0002 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01258 | hp1 | a0004 | c0011 | t0001 | g0184 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01258 | hp2 | a0013 | c0018 | t0002 | g0010 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01346 | hp2 | a0047 | c0094 | t0001 | g0283 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01358 | hp1 | a0048 | c0075 | t0002 | g0058 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01361 | hp1 | a0010 | c0010 | t0002 | g0032 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01361 | hp2 | a0049 | c0055 | t0002 | g0070 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01433 | hp1 | a0007 | c0004 | t0001 | g0310 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01433 | hp2 | a0050 | c0102 | t0001 | g0106 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01496 | hp2 | a0002 | c0019 | t0002 | g0064 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01515 | hp1 | a0006 | c0045 | t0001 | g0329 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01515 | hp2 | a0033 | c0049 | t0002 | g0245 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01516 | hp1 | a0010 | c0010 | t0002 | g0009 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01516 | hp2 | a0051 | c0104 | t0001 | g0300 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01517 | hp1 | a0010 | c0010 | t0002 | g0009 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01517 | hp2 | a0033 | c0049 | t0002 | g0246 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01884 | hp1 | a0024 | c0052 | t0002 | g0018 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01884 | hp2 | a0006 | c0006 | t0001 | g0330 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01891 | hp1 | a0032 | c0050 | t0002 | g0026 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01891 | hp2 | a0052 | c0116 | t0001 | g0370 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01934 | hp1 | a0053 | c0118 | t0002 | g0020 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01934 | hp2 | a0001 | c0007 | t0001 | g0304 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01943 | hp1 | a0002 | c0012 | t0002 | g0069 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01952 | hp1 | a0005 | c0024 | t0001 | g0220 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01952 | hp2 | a0018 | c0021 | t0002 | g0252 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01975 | hp1 | a0025 | c0033 | t0002 | g0155 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01978 | hp1 | a0018 | c0021 | t0002 | g0250 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01993 | hp1 | a0013 | c0018 | t0002 | g0097 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01993 | hp2 | a0002 | c0019 | t0002 | g0003 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02004 | hp1 | a0025 | c0033 | t0002 | g0152 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02027 | hp1 | a0005 | c0013 | t0001 | g0045 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02027 | hp2 | a0002 | c0012 | t0002 | g0042 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02040 | hp1 | a0004 | c0011 | t0001 | g0178 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02040 | hp2 | a0003 | c0003 | t0002 | g0365 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02055 | hp1 | a0009 | c0069 | t0001 | g0079 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02055 | hp2 | a0011 | c0009 | t0002 | g0141 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02071 | hp1 | a0054 | c0083 | t0002 | g0154 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02071 | hp2 | a0055 | c0111 | t0001 | g0271 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02080 | hp1 | a0006 | c0006 | t0001 | g0318 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02080 | hp2 | a0011 | c0009 | t0002 | g0061 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02083 | hp1 | a0003 | c0113 | t0002 | g0361 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02083 | hp2 | a0056 | c0054 | t0002 | g0158 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02129 | hp1 | a0058 | c0105 | t0001 | g0200 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02129 | hp2 | a0021 | c0027 | t0001 | g0008 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02132 | hp1 | a0005 | c0023 | t0001 | g0234 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02132 | hp2 | a0009 | c0020 | t0001 | g0075 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02145 | hp1 | a0009 | c0029 | t0001 | g0080 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02145 | hp2 | a0002 | c0042 | t0002 | g0081 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02148 | hp1 | a0025 | c0033 | t0002 | g0153 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02148 | hp2 | a0011 | c0009 | t0002 | g0060 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02155 | hp2 | a0026 | c0036 | t0002 | g0012 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02165 | hp1 | a0003 | c0003 | t0002 | g0363 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02257 | hp1 | a0004 | c0008 | t0001 | g0014 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02257 | hp2 | a0017 | c0017 | t0003 | g0206 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02258 | hp1 | a0002 | c0040 | t0002 | g0086 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02258 | hp2 | a0004 | c0008 | t0001 | g0177 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02280 | hp1 | a0006 | c0006 | t0001 | g0312 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02280 | hp2 | a0019 | c0022 | t0002 | g0335 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02293 | hp1 | a0002 | c0012 | t0002 | g0067 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02293 | hp2 | a0015 | c0014 | t0001 | g0286 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02300 | hp1 | a0002 | c0012 | t0002 | g0068 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02451 | hp1 | a0059 | c0078 | t0001 | g0371 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02451 | hp2 | a0004 | c0008 | t0001 | g0038 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02523 | hp1 | a0003 | c0003 | t0002 | g0366 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02523 | hp2 | a0004 | c0011 | t0001 | g0179 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02572 | hp1 | a0061 | c0076 | t0002 | g0049 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02572 | hp2 | a0004 | c0008 | t0001 | g0211 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02602 | hp1 | a0006 | c0006 | t0001 | g0319 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02615 | hp1 | a0019 | c0022 | t0002 | g0337 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02615 | hp2 | a0062 | c0117 | t0002 | g0149 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02622 | hp1 | a0012 | c0015 | t0001 | g0326 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02622 | hp2 | a0010 | c0010 | t0002 | g0308 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02630 | hp1 | a0063 | c0099 | t0001 | g0313 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02630 | hp2 | a0004 | c0008 | t0001 | g0186 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02683 | hp1 | a0064 | c0074 | t0002 | g0072 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02683 | hp2 | a0065 | c0085 | t0002 | g0035 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02698 | hp1 | a0066 | c0057 | t0001 | g0217 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02698 | hp2 | a0067 | c0060 | t0001 | g0181 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02717 | hp1 | a0010 | c0087 | t0002 | g0046 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02717 | hp2 | a0004 | c0061 | t0001 | g0176 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02735 | hp1 | a0034 | c0044 | t0001 | g0017 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02735 | hp2 | a0011 | c0009 | t0002 | g0059 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02738 | hp1 | a0023 | c0032 | t0001 | g0188 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02738 | hp2 | a0022 | c0028 | t0002 | g0216 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02809 | hp1 | a0007 | c0004 | t0001 | g0196 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02809 | hp2 | a0024 | c0052 | t0002 | g0018 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02818 | hp1 | a0009 | c0029 | t0001 | g0073 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02818 | hp2 | a0004 | c0008 | t0001 | g0187 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02886 | hp1 | a0007 | c0004 | t0001 | g0193 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02886 | hp2 | a0035 | c0043 | t0002 | g0137 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02895 | hp1 | a0007 | c0004 | t0001 | g0199 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02895 | hp2 | a0009 | c0029 | t0001 | g0074 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02922 | hp1 | a0007 | c0004 | t0001 | g0001 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02922 | hp2 | a0068 | c0097 | t0002 | g0028 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02965 | hp1 | a0007 | c0004 | t0001 | g0339 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02965 | hp2 | a0027 | c0035 | t0001 | g0139 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02970 | hp1 | a0002 | c0042 | t0002 | g0142 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02970 | hp2 | a0024 | c0125 | t0002 | g0369 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02976 | hp1 | a0006 | c0045 | t0001 | g0328 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02976 | hp2 | a0004 | c0011 | t0001 | g0162 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03017 | hp1 | a0026 | c0053 | t0002 | g0161 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03041 | hp1 | a0007 | c0004 | t0001 | g0185 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03041 | hp2 | a0004 | c0008 | t0001 | g0309 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03098 | hp1 | a0069 | c0065 | t0002 | g0175 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03098 | hp2 | a0035 | c0043 | t0002 | g0037 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03130 | hp1 | a0009 | c0091 | t0001 | g0048 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03130 | hp2 | a0019 | c0022 | t0002 | g0336 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03139 | hp1 | a0010 | c0010 | t0002 | g0025 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03139 | hp2 | a0007 | c0004 | t0001 | g0001 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03195 | hp1 | a0028 | c0068 | t0001 | g0173 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03195 | hp2 | a0019 | c0022 | t0002 | g0333 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03209 | hp1 | a0004 | c0011 | t0001 | g0190 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03209 | hp2 | a0012 | c0098 | t0001 | g0325 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03239 | hp1 | a0012 | c0015 | t0001 | g0323 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03453 | hp1 | a0070 | c0079 | t0001 | g0372 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03453 | hp2 | a0011 | c0009 | t0002 | g0062 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03486 | hp1 | a0027 | c0035 | t0001 | g0056 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03486 | hp2 | a0028 | c0037 | t0001 | g0013 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03491 | hp1 | a0022 | c0028 | t0002 | g0215 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03491 | hp2 | a0036 | c0046 | t0001 | g0264 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03492 | hp1 | a0037 | c0041 | t0001 | g0040 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03492 | hp2 | a0022 | c0028 | t0002 | g0214 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03516 | hp1 | a0004 | c0008 | t0001 | g0138 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03516 | hp2 | a0006 | c0006 | t0001 | g0314 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03540 | hp1 | a0007 | c0004 | t0001 | g0194 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03540 | hp2 | a0002 | c0095 | t0001 | g0134 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03579 | hp1 | a0072 | c0114 | t0001 | g0140 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03579 | hp2 | a0073 | c0123 | t0004 | g0225 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03654 | hp1 | a0022 | c0028 | t0002 | g0213 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03654 | hp2 | a0001 | c0109 | t0001 | g0244 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03704 | hp1 | a0006 | c0006 | t0001 | g0316 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03704 | hp2 | a0074 | c0082 | t0002 | g0085 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03710 | hp1 | a0036 | c0046 | t0001 | g0260 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03710 | hp2 | a0020 | c0026 | t0001 | g0172 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03831 | hp1 | a0037 | c0041 | t0001 | g0146 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03831 | hp2 | a0075 | c0056 | t0001 | g0212 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03834 | hp1 | a0076 | c0064 | t0001 | g0338 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03834 | hp2 | a0077 | c0107 | t0002 | g0277 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03927 | hp1 | a0006 | c0006 | t0001 | g0311 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03927 | hp2 | a0020 | c0026 | t0001 | g0164 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04115 | hp1 | a0004 | c0011 | t0001 | g0192 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04115 | hp2 | a0006 | c0006 | t0001 | g0315 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04199 | hp1 | a0078 | c0106 | t0002 | g0269 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04199 | hp2 | a0011 | c0009 | t0002 | g0057 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04204 | hp2 | a0034 | c0044 | t0001 | g0017 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04228 | hp2 | a0020 | c0026 | t0001 | g0157 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18522 | hp1 | a0028 | c0037 | t0001 | g0013 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18522 | hp2 | a0006 | c0006 | t0001 | g0331 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18612 | hp1 | a0006 | c0006 | t0001 | g0218 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0249 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18747 | hp2 | a0080 | c0101 | t0001 | g0108 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18906 | hp1 | a0081 | c0062 | t0001 | g0039 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18906 | hp2 | a0019 | c0022 | t0002 | g0334 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18939 | hp1 | a0029 | c0031 | t0001 | g0166 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18940 | hp2 | a0038 | c0047 | t0002 | g0353 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18941 | hp1 | a0020 | c0058 | t0001 | g0165 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18943 | hp1 | a0082 | c0108 | t0002 | g0364 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0342 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18945 | hp1 | a0005 | c0024 | t0001 | g0253 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18945 | hp2 | a0008 | c0005 | t0002 | g0004 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18948 | hp1 | a0012 | c0015 | t0001 | g0320 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18948 | hp2 | a0001 | c0007 | t0001 | g0274 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18949 | hp1 | a0001 | c0007 | t0001 | g0284 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18949 | hp2 | a0083 | c0112 | t0002 | g0341 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18950 | hp1 | a0001 | c0007 | t0001 | g0278 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18951 | hp1 | a0005 | c0013 | t0001 | g0233 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18951 | hp2 | a0009 | c0020 | t0001 | g0076 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18954 | hp2 | a0026 | c0036 | t0002 | g0012 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18956 | hp1 | a0015 | c0014 | t0001 | g0295 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18956 | hp2 | a0002 | c0093 | t0001 | g0129 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18961 | hp1 | a0005 | c0023 | t0001 | g0229 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18962 | hp1 | a0001 | c0007 | t0001 | g0282 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18963 | hp1 | a0015 | c0014 | t0001 | g0296 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18963 | hp2 | a0008 | c0005 | t0002 | g0099 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18967 | hp1 | a0015 | c0014 | t0001 | g0297 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18967 | hp2 | a0003 | c0048 | t0002 | g0352 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18970 | hp1 | a0015 | c0014 | t0001 | g0287 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18970 | hp2 | a0039 | c0038 | t0002 | g0095 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18972 | hp1 | a0014 | c0016 | t0002 | g0349 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18972 | hp2 | a0005 | c0013 | t0001 | g0239 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18973 | hp1 | a0003 | c0003 | t0002 | g0359 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18975 | hp1 | a0001 | c0007 | t0001 | g0280 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18977 | hp1 | a0030 | c0030 | t0001 | g0170 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18977 | hp2 | a0005 | c0013 | t0001 | g0228 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18980 | hp2 | a0002 | c0096 | t0002 | g0044 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18982 | hp1 | a0003 | c0003 | t0002 | g0053 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18984 | hp1 | a0008 | c0005 | t0002 | g0147 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18985 | hp1 | a0040 | c0039 | t0002 | g0083 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18985 | hp2 | a0005 | c0023 | t0001 | g0230 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18989 | hp1 | a0002 | c0012 | t0002 | g0082 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18990 | hp1 | a0014 | c0016 | t0002 | g0347 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18990 | hp2 | a0008 | c0005 | t0002 | g0047 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18993 | hp1 | a0005 | c0024 | t0001 | g0223 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18995 | hp2 | a0008 | c0005 | t0002 | g0101 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18998 | hp1 | a0003 | c0003 | t0002 | g0307 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18998 | hp2 | a0086 | c0084 | t0001 | g0123 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18999 | hp1 | a0038 | c0047 | t0002 | g0358 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18999 | hp2 | a0015 | c0014 | t0001 | g0306 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19000 | hp1 | a0005 | c0013 | t0001 | g0232 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19000 | hp2 | a0001 | c0007 | t0001 | g0273 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19002 | hp1 | a0004 | c0011 | t0001 | g0198 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19002 | hp2 | a0008 | c0005 | t0002 | g0103 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19004 | hp1 | a0030 | c0030 | t0001 | g0169 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19005 | hp2 | a0021 | c0027 | t0001 | g0008 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19007 | hp1 | a0009 | c0020 | t0001 | g0078 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19007 | hp2 | a0003 | c0003 | t0002 | g0346 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19009 | hp1 | a0014 | c0016 | t0006 | g0368 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19011 | hp1 | a0003 | c0003 | t0002 | g0343 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19011 | hp2 | a0001 | c0007 | t0001 | g0281 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19030 | hp1 | a0010 | c0010 | t0002 | g0024 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19030 | hp2 | a0087 | c0124 | t0002 | g0071 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19054 | hp1 | a0029 | c0031 | t0001 | g0204 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19054 | hp2 | a0008 | c0005 | t0002 | g0063 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19055 | hp1 | a0001 | c0007 | t0001 | g0279 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19055 | hp2 | a0030 | c0030 | t0001 | g0168 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19056 | hp2 | a0020 | c0026 | t0001 | g0167 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19057 | hp1 | a0005 | c0013 | t0001 | g0237 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0344 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19058 | hp1 | a0005 | c0023 | t0001 | g0235 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19060 | hp1 | a0040 | c0039 | t0002 | g0091 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19060 | hp2 | a0088 | c0072 | t0001 | g0290 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19062 | hp2 | a0008 | c0005 | t0002 | g0004 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19064 | hp1 | a0039 | c0038 | t0002 | g0096 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0367 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19065 | hp1 | a0005 | c0024 | t0001 | g0221 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19066 | hp1 | a0012 | c0015 | t0001 | g0324 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19067 | hp1 | a0005 | c0023 | t0001 | g0236 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19068 | hp2 | a0013 | c0018 | t0002 | g0092 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19070 | hp1 | a0003 | c0003 | t0002 | g0360 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19074 | hp1 | a0013 | c0018 | t0002 | g0093 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19078 | hp1 | a0014 | c0016 | t0002 | g0348 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19078 | hp2 | a0089 | c0090 | t0002 | g0143 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19079 | hp1 | a0005 | c0024 | t0001 | g0219 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19079 | hp2 | a0008 | c0005 | t0002 | g0102 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0356 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19080 | hp2 | a0021 | c0027 | t0001 | g0008 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19081 | hp1 | a0029 | c0031 | t0001 | g0171 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19081 | hp2 | a0090 | c0073 | t0001 | g0118 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0355 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19082 | hp2 | a0001 | c0110 | t0001 | g0268 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19083 | hp2 | a0008 | c0005 | t0002 | g0104 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19085 | hp1 | a0008 | c0005 | t0002 | g0098 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19086 | hp2 | a0003 | c0048 | t0005 | g0362 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19087 | hp1 | a0008 | c0005 | t0002 | g0100 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19089 | hp1 | a0008 | c0005 | t0002 | g0340 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19089 | hp2 | a0005 | c0013 | t0001 | g0231 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19090 | hp1 | a0002 | c0012 | t0002 | g0066 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19240 | hp1 | a0012 | c0015 | t0001 | g0321 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19240 | hp2 | a0009 | c0029 | t0001 | g0055 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20129 | hp1 | a0091 | c0067 | t0002 | g0203 | AFR | ASW | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20129 | hp2 | a0092 | c0121 | t0001 | g0222 | AFR | ASW | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20752 | hp1 | a0094 | c0100 | t0001 | g0322 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20752 | hp2 | a0095 | c0092 | t0001 | g0144 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20805 | hp1 | a0001 | c0007 | t0001 | g0276 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20805 | hp2 | a0011 | c0009 | t0002 | g0002 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0124 | SAS | GIH | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20905 | hp2 | a0017 | c0017 | t0003 | g0208 | SAS | GIH | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01123 | hp1 | a0017 | c0017 | t0003 | g0207 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02109 | hp1 | a0010 | c0010 | t0001 | g0022 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02109 | hp2 | a0057 | c0122 | t0004 | g0226 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02486 | hp1 | a0027 | c0035 | t0001 | g0021 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02486 | hp2 | a0006 | c0006 | t0001 | g0332 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02559 | hp1 | a0060 | c0077 | t0001 | g0132 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02559 | hp2 | a0001 | c0034 | t0001 | g0261 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03471 | hp1 | a0071 | c0115 | t0001 | g0054 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03471 | hp2 | a0021 | c0027 | t0001 | g0174 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG06807 | hp1 | a0012 | c0015 | t0001 | g0327 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG06807 | hp2 | a0079 | c0081 | t0002 | g0019 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18955 | hp1 | a0084 | c0086 | t0001 | g0131 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18955 | hp2 | a0085 | c0059 | t0001 | g0163 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20300 | hp1 | a0018 | c0021 | t0002 | g0302 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20300 | hp2 | a0093 | c0119 | t0004 | g0227 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA21309 | hp1 | a0008 | c0005 | t0002 | g0004 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA21309 | hp2 | a0096 | c0063 | t0001 | g0148 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
homoSapiens | chm13v2 | a0097 | c0103 | t0001 | g0263 | REF | REF | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041874 | C | T | 1 | a0033 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.12530G>A | p.Ser4177Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12696/13097 | 12530/12735 | 4177/4244 | chr6 | 32041874 | |||
chr6:32041884 | C | T | 1 | a0033 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.12520G>A | p.Asp4174Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12686/13097 | 12520/12735 | 4174/4244 | chr6 | 32041884 | |||
chr6:32041892 | C | T | 1 | a0024 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.12512G>A | p.Arg4171His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12678/13097 | 12512/12735 | 4171/4244 | chr6 | 32041892 | |||
chr6:32042495 | T | A | 12 | a0001 a0015 a0033 others(9): Show |
80 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(77): Show |
missense_variant | MODERATE | c.12170A>T | p.Asn4057Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12336/13097 | 12170/12735 | 4057/4244 | chr6 | 32042495 | |||
chr6:32042522 | A | T | 1 | a0063 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.12143T>A | p.Leu4048His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12309/13097 | 12143/12735 | 4048/4244 | chr6 | 32042522 | |||
chr6:32042746 | A | G | 10 | a0006 a0012 a0019 others(7): Show |
36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
missense_variant | MODERATE | c.12011T>C | p.Met4004Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/44 | 12177/13097 | 12011/12735 | 4004/4244 | chr6 | 32042746 | |||
chr6:32042955 | T | G | 27 | a0001 a0006 a0012 others(24): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
missense_variant | MODERATE | c.11921A>C | p.Asn3974Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/44 | 12087/13097 | 11921/12735 | 3974/4244 | chr6 | 32042955 | |||
chr6:32043073 | C | T | 2 | a0028 a0046 |
4 | HG01243.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.11803G>A | p.Ala3935Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/44 | 11969/13097 | 11803/12735 | 3935/4244 | chr6 | 32043073 | |||
chr6:32043458 | C | T | 39 | a0001 a0004 a0005 others(36): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
missense_variant | MODERATE | c.11629G>A | p.Val3877Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11795/13097 | 11629/12735 | 3877/4244 | chr6 | 32043458 | |||
chr6:32043539 | G | T | 15 | a0005 a0008 a0017 others(12): Show |
59 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(56): Show |
missense_variant | MODERATE | c.11548C>A | p.Gln3850Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11714/13097 | 11548/12735 | 3850/4244 | chr6 | 32043539 | |||
chr6:32043718 | ACCTCTTG others(113): Show |
A | 1 | a0082 | 1 | NA18943.hp1 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.11441_11530+30del | p.Gly3814_Thr3843del | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11441/12735 | 3814/4244 | chr6 | 32043718 | ||||
chr6:32043862 | T | C | 2 | a0072 a0074 |
2 | HG03579.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.11417A>G | p.Gln3806Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11583/13097 | 11417/12735 | 3806/4244 | chr6 | 32043862 | |||
chr6:32044483 | G | A | 2 | a0013 a0040 |
8 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.11161C>T | p.Arg3721Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11327/13097 | 11161/12735 | 3721/4244 | chr6 | 32044483 | |||
chr6:32044684 | A | C | 8 | a0003 a0014 a0018 others(5): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
missense_variant | MODERATE | c.10960T>G | p.Ser3654Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11126/13097 | 10960/12735 | 3654/4244 | chr6 | 32044684 | |||
chr6:32045029 | G | T | 1 | a0043 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.10904C>A | p.Pro3635His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 11070/13097 | 10904/12735 | 3635/4244 | chr6 | 32045029 | |||
chr6:32045120 | C | T | 2 | a0057 a0073 |
2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.10813G>A | p.Asp3605Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 10979/13097 | 10813/12735 | 3605/4244 | chr6 | 32045120 | |||
chr6:32046196 | C | T | 1 | a0081 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.10585G>A | p.Val3529Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10751/13097 | 10585/12735 | 3529/4244 | chr6 | 32046196 | |||
chr6:32046198 | G | A | 1 | a0024 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.10583C>T | p.Pro3528Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10749/13097 | 10583/12735 | 3528/4244 | chr6 | 32046198 | |||
chr6:32046292 | C | T | 1 | a0078 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.10489G>A | p.Ala3497Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10655/13097 | 10489/12735 | 3497/4244 | chr6 | 32046292 | |||
chr6:32046421 | C | T | 1 | a0084 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.10360G>A | p.Glu3454Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10526/13097 | 10360/12735 | 3454/4244 | chr6 | 32046421 | |||
chr6:32047988 | C | T | 1 | a0067 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.10070G>A | p.Arg3357His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/44 | 10236/13097 | 10070/12735 | 3357/4244 | chr6 | 32047988 | |||
chr6:32047998 | G | A | 1 | a0018 | 5 | HG01167.hp1 HG01192.hp1 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.10060C>T | p.Pro3354Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/44 | 10226/13097 | 10060/12735 | 3354/4244 | chr6 | 32047998 | |||
chr6:32048363 | C | G | 1 | a0055 | 1 | HG02071.hp2 | missense_variant&splice_region_variant | MODERATE | c.10045G>C | p.Ala3349Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 10211/13097 | 10045/12735 | 3349/4244 | chr6 | 32048363 | |||
chr6:32049366 | C | T | 1 | a0066 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.9661G>A | p.Val3221Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9827/13097 | 9661/12735 | 3221/4244 | chr6 | 32049366 | |||
chr6:32049384 | C | T | 3 | a0005 a0043 a0092 |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.9643G>A | p.Glu3215Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9809/13097 | 9643/12735 | 3215/4244 | chr6 | 32049384 | |||
chr6:32049386 | C | A | 1 | a0011 | 10 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(7): Show |
missense_variant | MODERATE | c.9641G>T | p.Gly3214Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9807/13097 | 9641/12735 | 3214/4244 | chr6 | 32049386 | |||
chr6:32049396 | G | C | 2 | a0041 a0095 |
2 | HG00140.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.9631C>G | p.Arg3211Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9797/13097 | 9631/12735 | 3211/4244 | chr6 | 32049396 | |||
chr6:32049456 | C | T | 2 | a0028 a0046 |
4 | HG01243.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.9571G>A | p.Gly3191Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9737/13097 | 9571/12735 | 3191/4244 | chr6 | 32049456 | |||
chr6:32049465 | C | T | 3 | a0006 a0028 a0046 |
18 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(15): Show |
missense_variant | MODERATE | c.9562G>A | p.Val3188Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9728/13097 | 9562/12735 | 3188/4244 | chr6 | 32049465 | |||
chr6:32049501 | C | T | 1 | a0058 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.9526G>A | p.Gly3176Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9692/13097 | 9526/12735 | 3176/4244 | chr6 | 32049501 | |||
chr6:32050249 | A | C | 1 | a0051 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.9188T>G | p.Leu3063Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/44 | 9354/13097 | 9188/12735 | 3063/4244 | chr6 | 32050249 | |||
chr6:32052700 | C | T | 1 | a0067 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.9085G>A | p.Val3029Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9251/13097 | 9085/12735 | 3029/4244 | chr6 | 32052700 | |||
chr6:32052745 | A | G | 1 | a0034 | 2 | HG02735.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.9040T>C | p.Cys3014Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9206/13097 | 9040/12735 | 3014/4244 | chr6 | 32052745 | |||
chr6:32053418 | C | T | 1 | a0038 | 2 | NA18940.hp2 NA18999.hp1 |
missense_variant | MODERATE | c.8761G>A | p.Val2921Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8927/13097 | 8761/12735 | 2921/4244 | chr6 | 32053418 | |||
chr6:32053499 | C | T | 2 | a0025 a0053 |
4 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
missense_variant | MODERATE | c.8680G>A | p.Glu2894Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8846/13097 | 8680/12735 | 2894/4244 | chr6 | 32053499 | |||
chr6:32053585 | A | G | 3 | a0005 a0043 a0092 |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.8594T>C | p.Met2865Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8760/13097 | 8594/12735 | 2865/4244 | chr6 | 32053585 | |||
chr6:32055974 | C | CACGCATC others(8): Show |
1 | a0086 | 1 | NA18998.hp2 | conservative_inframe_insertion | MODERATE | c.8329_8343dupCCCCAG others(9): Show |
p.Arg2781_Val2782ins others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8509/13097 | 8343/12735 | 2781/4244 | chr6 | 32055974 | |||
chr6:32056108 | G | A | 1 | a0071 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.8210C>T | p.Pro2737Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8376/13097 | 8210/12735 | 2737/4244 | chr6 | 32056108 | |||
chr6:32056126 | G | C | 5 | a0010 a0031 a0032 others(2): Show |
17 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(14): Show |
missense_variant | MODERATE | c.8192C>G | p.Pro2731Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8358/13097 | 8192/12735 | 2731/4244 | chr6 | 32056126 | |||
chr6:32056592 | C | A | 1 | a0061 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.8137G>T | p.Val2713Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8303/13097 | 8137/12735 | 2713/4244 | chr6 | 32056592 | |||
chr6:32056616 | C | T | 1 | a0040 | 2 | NA18985.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.8113G>A | p.Val2705Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8279/13097 | 8113/12735 | 2705/4244 | chr6 | 32056616 | |||
chr6:32056618 | C | T | 10 | a0009 a0027 a0041 others(7): Show |
22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
missense_variant | MODERATE | c.8111G>A | p.Arg2704His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8277/13097 | 8111/12735 | 2704/4244 | chr6 | 32056618 | |||
chr6:32056775 | C | T | 1 | a0054 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.7954G>A | p.Glu2652Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8120/13097 | 7954/12735 | 2652/4244 | chr6 | 32056775 | |||
chr6:32056783 | G | A | 2 | a0045 a0083 |
2 | HG00673.hp2 NA18949.hp2 |
missense_variant | MODERATE | c.7946C>T | p.Thr2649Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8112/13097 | 7946/12735 | 2649/4244 | chr6 | 32056783 | |||
chr6:32058081 | G | A | 1 | a0044 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.7802C>T | p.Pro2601Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7968/13097 | 7802/12735 | 2601/4244 | chr6 | 32058081 | |||
chr6:32058093 | C | T | 19 | a0004 a0005 a0007 others(16): Show |
87 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(84): Show |
missense_variant | MODERATE | c.7790G>A | p.Arg2597Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7956/13097 | 7790/12735 | 2597/4244 | chr6 | 32058093 | |||
chr6:32058155 | AGTGACCT others(3332): Show |
A | 1 | a0019 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
conservative_inframe_deletion | MODERATE | c.7395_7727del | p.Thr2465_Val2575del | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7893/13097 | 7395/12735 | 2465/4244 | chr6 | 32058155 | |||
chr6:32058250 | G | A | 1 | a0016 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.7633C>T | p.Pro2545Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7799/13097 | 7633/12735 | 2545/4244 | chr6 | 32058250 | |||
chr6:32058330 | C | T | 62 | a0001 a0002 a0003 others(59): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
missense_variant | MODERATE | c.7553G>A | p.Gly2518Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7719/13097 | 7553/12735 | 2518/4244 | chr6 | 32058330 | |||
chr6:32061406 | C | T | 14 | a0004 a0007 a0017 others(11): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
missense_variant | MODERATE | c.7483G>A | p.Gly2495Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7649/13097 | 7483/12735 | 2495/4244 | chr6 | 32061406 | |||
chr6:32061472 | G | A | 1 | a0020 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.7417C>T | p.Arg2473Cys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7583/13097 | 7417/12735 | 2473/4244 | chr6 | 32061472 | |||
chr6:32061528 | A | G | 1 | a0019 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.7361T>C | p.Val2454Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7527/13097 | 7361/12735 | 2454/4244 | chr6 | 32061528 | |||
chr6:32061537 | C | T | 1 | a0036 | 2 | HG03491.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.7352G>A | p.Arg2451Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7518/13097 | 7352/12735 | 2451/4244 | chr6 | 32061537 | |||
chr6:32061541 | C | T | 1 | a0075 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.7348G>A | p.Gly2450Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7514/13097 | 7348/12735 | 2450/4244 | chr6 | 32061541 | |||
chr6:32061542 | G | C | 1 | a0056 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.7347C>G | p.Asp2449Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7513/13097 | 7347/12735 | 2449/4244 | chr6 | 32061542 | |||
chr6:32061592 | C | T | 1 | a0024 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.7297G>A | p.Val2433Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7463/13097 | 7297/12735 | 2433/4244 | chr6 | 32061592 | |||
chr6:32061654 | G | A | 10 | a0009 a0027 a0041 others(7): Show |
22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
missense_variant | MODERATE | c.7235C>T | p.Pro2412Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7401/13097 | 7235/12735 | 2412/4244 | chr6 | 32061654 | |||
chr6:32062274 | C | T | 1 | a0070 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.7051G>A | p.Gly2351Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7217/13097 | 7051/12735 | 2351/4244 | chr6 | 32062274 | |||
chr6:32062354 | G | T | 2 | a0052 a0059 |
2 | HG01891.hp2 HG02451.hp1 |
missense_variant | MODERATE | c.6971C>A | p.Thr2324Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7137/13097 | 6971/12735 | 2324/4244 | chr6 | 32062354 | |||
chr6:32062423 | G | T | 3 | a0005 a0043 a0092 |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.6902C>A | p.Pro2301His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7068/13097 | 6902/12735 | 2301/4244 | chr6 | 32062423 | |||
chr6:32064851 | C | G | 1 | a0008 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
missense_variant | MODERATE | c.6811G>C | p.Val2271Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6977/13097 | 6811/12735 | 2271/4244 | chr6 | 32064851 | |||
chr6:32064968 | C | T | 1 | a0039 | 2 | NA18970.hp2 NA19064.hp1 |
missense_variant | MODERATE | c.6694G>A | p.Asp2232Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6860/13097 | 6694/12735 | 2232/4244 | chr6 | 32064968 | |||
chr6:32064979 | A | T | 6 | a0005 a0043 a0057 others(3): Show |
22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
missense_variant | MODERATE | c.6683T>A | p.Phe2228Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6849/13097 | 6683/12735 | 2228/4244 | chr6 | 32064979 | |||
chr6:32065054 | C | T | 1 | a0014 | 6 | HG00408.hp2 HG00609.hp2 NA18972.hp1 others(3): Show |
missense_variant | MODERATE | c.6608G>A | p.Arg2203Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6774/13097 | 6608/12735 | 2203/4244 | chr6 | 32065054 | |||
chr6:32067697 | G | A | 1 | a0092 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.6508C>T | p.Arg2170Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6674/13097 | 6508/12735 | 2170/4244 | chr6 | 32067697 | |||
chr6:32067777 | C | T | 1 | a0057 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.6428G>A | p.Gly2143Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6594/13097 | 6428/12735 | 2143/4244 | chr6 | 32067777 | |||
chr6:32067826 | C | T | 17 | a0004 a0007 a0017 others(14): Show |
71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
missense_variant | MODERATE | c.6379G>A | p.Val2127Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6545/13097 | 6379/12735 | 2127/4244 | chr6 | 32067826 | |||
chr6:32068672 | C | T | 2 | a0046 a0060 |
2 | HG01243.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.5938G>A | p.Ala1980Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6104/13097 | 5938/12735 | 1980/4244 | chr6 | 32068672 | |||
chr6:32068945 | T | C | 1 | a0085 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.5779A>G | p.Ile1927Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5945/13097 | 5779/12735 | 1927/4244 | chr6 | 32068945 | |||
chr6:32068978 | T | C | 1 | a0035 | 2 | HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.5746A>G | p.Thr1916Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5912/13097 | 5746/12735 | 1916/4244 | chr6 | 32068978 | |||
chr6:32069011 | C | T | 1 | a0007 | 14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
missense_variant | MODERATE | c.5713G>A | p.Glu1905Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5879/13097 | 5713/12735 | 1905/4244 | chr6 | 32069011 | |||
chr6:32069592 | C | T | 1 | a0024 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.5548G>A | p.Gly1850Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5714/13097 | 5548/12735 | 1850/4244 | chr6 | 32069592 | |||
chr6:32069698 | G | C | 1 | a0029 | 3 | NA18939.hp1 NA19054.hp1 NA19081.hp1 |
missense_variant | MODERATE | c.5442C>G | p.Asp1814Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5608/13097 | 5442/12735 | 1814/4244 | chr6 | 32069698 | |||
chr6:32069724 | A | G | 1 | a0050 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.5416T>C | p.Phe1806Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5582/13097 | 5416/12735 | 1806/4244 | chr6 | 32069724 | |||
chr6:32070362 | C | T | 1 | a0080 | 1 | NA18747.hp2 | stop_gained | HIGH | c.5043G>A | p.Trp1681* | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/44 | 5209/13097 | 5043/12735 | 1681/4244 | chr6 | 32070362 | |||
chr6:32072095 | C | T | 3 | a0005 a0043 a0092 |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.4885G>A | p.Glu1629Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/44 | 5051/13097 | 4885/12735 | 1629/4244 | chr6 | 32072095 | |||
chr6:32072218 | T | C | 1 | a0037 | 2 | HG03492.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.4762A>G | p.Ile1588Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/44 | 4928/13097 | 4762/12735 | 1588/4244 | chr6 | 32072218 | |||
chr6:32073766 | G | A | 2 | a0048 a0061 |
2 | HG01358.hp1 HG02572.hp1 |
missense_variant | MODERATE | c.4562C>T | p.Ala1521Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4728/13097 | 4562/12735 | 1521/4244 | chr6 | 32073766 | |||
chr6:32073844 | G | A | 2 | a0031 a0068 |
3 | HG00642.hp1 HG01081.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.4484C>T | p.Thr1495Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4650/13097 | 4484/12735 | 1495/4244 | chr6 | 32073844 | |||
chr6:32073896 | C | T | 1 | a0060 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4432G>A | p.Gly1478Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4598/13097 | 4432/12735 | 1478/4244 | chr6 | 32073896 | |||
chr6:32079167 | C | T | 6 | a0011 a0026 a0048 others(3): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
missense_variant | MODERATE | c.4241G>A | p.Arg1414Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4407/13097 | 4241/12735 | 1414/4244 | chr6 | 32079167 | |||
chr6:32079291 | G | T | 1 | a0064 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.4117C>A | p.Pro1373Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4283/13097 | 4117/12735 | 1373/4244 | chr6 | 32079291 | |||
chr6:32081646 | C | G | 1 | a0090 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.3764G>C | p.Arg1255Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3930/13097 | 3764/12735 | 1255/4244 | chr6 | 32081646 | |||
chr6:32081646 | C | T | 6 | a0006 a0012 a0034 others(3): Show |
26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
missense_variant | MODERATE | c.3764G>A | p.Arg1255His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3930/13097 | 3764/12735 | 1255/4244 | chr6 | 32081646 | |||
chr6:32081652 | G | T | 2 | a0057 a0073 |
2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.3758C>A | p.Pro1253His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3924/13097 | 3758/12735 | 1253/4244 | chr6 | 32081652 | |||
chr6:32082290 | T | C | 49 | a0001 a0003 a0004 others(46): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(239): Show |
missense_variant | MODERATE | c.3482A>G | p.His1161Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/44 | 3648/13097 | 3482/12735 | 1161/4244 | chr6 | 32082290 | |||
chr6:32084449 | T | C | 1 | a0088 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.3409A>G | p.Lys1137Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3575/13097 | 3409/12735 | 1137/4244 | chr6 | 32084449 | |||
chr6:32084478 | T | C | 3 | a0027 a0071 a0072 |
5 | HG02486.hp1 HG02965.hp2 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.3380A>G | p.Lys1127Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3546/13097 | 3380/12735 | 1127/4244 | chr6 | 32084478 | |||
chr6:32084586 | G | T | 3 | a0057 a0073 a0093 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.3272C>A | p.Ser1091Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3438/13097 | 3272/12735 | 1091/4244 | chr6 | 32084586 | |||
chr6:32084632 | C | T | 1 | a0041 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.3226G>A | p.Asp1076Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3392/13097 | 3226/12735 | 1076/4244 | chr6 | 32084632 | |||
chr6:32084667 | C | T | 1 | a0042 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.3191G>A | p.Arg1064His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3357/13097 | 3191/12735 | 1064/4244 | chr6 | 32084667 | |||
chr6:32085951 | C | T | 1 | a0096 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2947G>A | p.Ala983Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/44 | 3113/13097 | 2947/12735 | 983/4244 | chr6 | 32085951 | |||
chr6:32088803 | A | C | 18 | a0004 a0007 a0017 others(15): Show |
72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
missense_variant | MODERATE | c.2761T>G | p.Ser921Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/44 | 2927/13097 | 2761/12735 | 921/4244 | chr6 | 32088803 | |||
chr6:32088848 | C | A | 1 | a0032 | 2 | HG00735.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.2716G>T | p.Val906Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/44 | 2882/13097 | 2716/12735 | 906/4244 | chr6 | 32088848 | |||
chr6:32089349 | G | A | 1 | a0052 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2389C>T | p.Arg797Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2555/13097 | 2389/12735 | 797/4244 | chr6 | 32089349 | |||
chr6:32095878 | G | A | 1 | a0053 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1975C>T | p.Arg659Cys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2141/13097 | 1975/12735 | 659/4244 | chr6 | 32095878 | |||
chr6:32095888 | G | C | 2 | a0057 a0073 |
2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1965C>G | p.Asp655Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2131/13097 | 1965/12735 | 655/4244 | chr6 | 32095888 | |||
chr6:32095904 | C | T | 7 | a0004 a0007 a0021 others(4): Show |
44 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(41): Show |
missense_variant | MODERATE | c.1949G>A | p.Arg650His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2115/13097 | 1949/12735 | 650/4244 | chr6 | 32095904 | |||
chr6:32095926 | T | C | 1 | a0031 | 2 | HG00642.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.1927A>G | p.Thr643Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2093/13097 | 1927/12735 | 643/4244 | chr6 | 32095926 | |||
chr6:32096016 | T | C | 6 | a0005 a0043 a0057 others(3): Show |
22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
missense_variant | MODERATE | c.1837A>G | p.Ser613Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2003/13097 | 1837/12735 | 613/4244 | chr6 | 32096016 | |||
chr6:32096321 | C | T | 17 | a0004 a0007 a0017 others(14): Show |
69 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(66): Show |
missense_variant | MODERATE | c.1532G>A | p.Arg511His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1698/13097 | 1532/12735 | 511/4244 | chr6 | 32096321 | |||
chr6:32096384 | C | T | 1 | a0015 | 6 | HG02293.hp2 NA18956.hp1 NA18963.hp1 others(3): Show |
missense_variant | MODERATE | c.1469G>A | p.Arg490Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1635/13097 | 1469/12735 | 490/4244 | chr6 | 32096384 | |||
chr6:32096594 | A | G | 1 | a0076 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1259T>C | p.Val420Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1425/13097 | 1259/12735 | 420/4244 | chr6 | 32096594 | |||
chr6:32096752 | G | C | 1 | a0087 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1101C>G | p.Asp367Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1267/13097 | 1101/12735 | 367/4244 | chr6 | 32096752 | |||
chr6:32096949 | T | C | 1 | a0016 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
missense_variant | MODERATE | c.904A>G | p.Thr302Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1070/13097 | 904/12735 | 302/4244 | chr6 | 32096949 | |||
chr6:32097234 | C | T | 1 | a0096 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.619G>A | p.Gly207Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 785/13097 | 619/12735 | 207/4244 | chr6 | 32097234 | |||
chr6:32097246 | C | T | 5 | a0004 a0007 a0023 others(2): Show |
39 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(36): Show |
missense_variant | MODERATE | c.607G>A | p.Val203Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 773/13097 | 607/12735 | 203/4244 | chr6 | 32097246 | |||
chr6:32097336 | C | T | 6 | a0020 a0029 a0030 others(3): Show |
14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
missense_variant | MODERATE | c.517G>A | p.Ala173Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 683/13097 | 517/12735 | 173/4244 | chr6 | 32097336 | |||
chr6:32098086 | C | T | 1 | a0049 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.113G>A | p.Arg38Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/44 | 279/13097 | 113/12735 | 38/4244 | chr6 | 32098086 | |||
chr6:32098113 | C | T | 2 | a0026 a0056 |
4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
missense_variant | MODERATE | c.86G>A | p.Arg29Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/44 | 252/13097 | 86/12735 | 29/4244 | chr6 | 32098113 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041421 | G | A | 1 | a0001c0109 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.12663C>T | p.Phe4221Phe | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 12829/13097 | 12663/12735 | 4221/4244 | chr6 | 32041421 | |||
chr6:32041792 | G | A | 1 | a0001c0110 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.12612C>T | p.Tyr4204Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12778/13097 | 12612/12735 | 4204/4244 | chr6 | 32041792 | |||
chr6:32042103 | G | A | 1 | a0008c0005 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
synonymous_variant | LOW | c.12378C>T | p.Asp4126Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 42/44 | 12544/13097 | 12378/12735 | 4126/4244 | chr6 | 32042103 | |||
chr6:32042509 | G | C | 4 | a0005c0013 a0005c0023 a0005c0024 others(1): Show |
18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
synonymous_variant | LOW | c.12156C>G | p.Arg4052Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12322/13097 | 12156/12735 | 4052/4244 | chr6 | 32042509 | |||
chr6:32043471 | C | T | 50 | a0001c0001 a0001c0007 a0001c0034 others(47): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
synonymous_variant | LOW | c.11616G>A | p.Val3872Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11782/13097 | 11616/12735 | 3872/4244 | chr6 | 32043471 | |||
chr6:32043540 | T | C | 18 | a0005c0013 a0005c0023 a0005c0024 others(15): Show |
59 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(56): Show |
synonymous_variant | LOW | c.11547A>G | p.Thr3849Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11713/13097 | 11547/12735 | 3849/4244 | chr6 | 32043540 | |||
chr6:32043867 | A | G | 25 | a0004c0008 a0004c0011 a0004c0061 others(22): Show |
85 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
synonymous_variant | LOW | c.11412T>C | p.Asp3804Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11578/13097 | 11412/12735 | 3804/4244 | chr6 | 32043867 | |||
chr6:32044502 | C | T | 6 | a0008c0005 a0010c0010 a0024c0125 others(3): Show |
30 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(27): Show |
synonymous_variant | LOW | c.11142G>A | p.Thr3714Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11308/13097 | 11142/12735 | 3714/4244 | chr6 | 32044502 | |||
chr6:32044556 | A | T | 16 | a0001c0001 a0001c0007 a0001c0109 others(13): Show |
78 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(75): Show |
synonymous_variant | LOW | c.11088T>A | p.Thr3696Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11254/13097 | 11088/12735 | 3696/4244 | chr6 | 32044556 | |||
chr6:32045040 | C | T | 4 | a0001c0007 a0047c0094 a0051c0104 others(1): Show |
15 | HG00639.hp1 HG00733.hp1 HG01346.hp2 others(12): Show |
synonymous_variant | LOW | c.10893G>A | p.Lys3631Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 11059/13097 | 10893/12735 | 3631/4244 | chr6 | 32045040 | |||
chr6:32045256 | T | C | 2 | a0004c0061 a0023c0032 |
4 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.10677A>G | p.Leu3559Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 10843/13097 | 10677/12735 | 3559/4244 | chr6 | 32045256 | |||
chr6:32046227 | G | A | 1 | a0009c0091 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.10554C>T | p.Tyr3518Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10720/13097 | 10554/12735 | 3518/4244 | chr6 | 32046227 | |||
chr6:32046413 | G | A | 3 | a0057c0122 a0073c0123 a0093c0119 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.10368C>T | p.Thr3456Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10534/13097 | 10368/12735 | 3456/4244 | chr6 | 32046413 | |||
chr6:32048559 | C | T | 1 | a0049c0055 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.9849G>A | p.Thr3283Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 10015/13097 | 9849/12735 | 3283/4244 | chr6 | 32048559 | |||
chr6:32048646 | G | A | 1 | a0026c0036 | 2 | HG02155.hp2 NA18954.hp2 |
synonymous_variant | LOW | c.9762C>T | p.Pro3254Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 9928/13097 | 9762/12735 | 3254/4244 | chr6 | 32048646 | |||
chr6:32049328 | A | G | 10 | a0002c0012 a0002c0019 a0002c0096 others(7): Show |
23 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
synonymous_variant | LOW | c.9699T>C | p.His3233His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9865/13097 | 9699/12735 | 3233/4244 | chr6 | 32049328 | |||
chr6:32049355 | C | T | 1 | a0006c0045 | 2 | HG01515.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.9672G>A | p.Leu3224Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9838/13097 | 9672/12735 | 3224/4244 | chr6 | 32049355 | |||
chr6:32049364 | C | T | 1 | a0005c0023 | 5 | HG02132.hp1 NA18961.hp1 NA18985.hp2 others(2): Show |
synonymous_variant | LOW | c.9663G>A | p.Val3221Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9829/13097 | 9663/12735 | 3221/4244 | chr6 | 32049364 | |||
chr6:32050269 | C | T | 1 | a0062c0117 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.9168G>A | p.Glu3056Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/44 | 9334/13097 | 9168/12735 | 3056/4244 | chr6 | 32050269 | |||
chr6:32052785 | G | A | 1 | a0056c0054 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.9000C>T | p.Gly3000Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9166/13097 | 9000/12735 | 3000/4244 | chr6 | 32052785 | |||
chr6:32053581 | G | A | 5 | a0005c0013 a0005c0023 a0005c0024 others(2): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.8598C>T | p.Val2866Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8764/13097 | 8598/12735 | 2866/4244 | chr6 | 32053581 | |||
chr6:32055855 | C | A | 1 | a0055c0111 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.8463G>T | p.Val2821Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8629/13097 | 8463/12735 | 2821/4244 | chr6 | 32055855 | |||
chr6:32056842 | A | G | 1 | a0013c0080 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.7887T>C | p.Pro2629Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8053/13097 | 7887/12735 | 2629/4244 | chr6 | 32056842 | |||
chr6:32056863 | G | A | 2 | a0005c0024 a0092c0121 |
6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
synonymous_variant | LOW | c.7866C>T | p.Thr2622Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8032/13097 | 7866/12735 | 2622/4244 | chr6 | 32056863 | |||
chr6:32058086 | C | T | 8 | a0002c0040 a0013c0018 a0013c0080 others(5): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
synonymous_variant | LOW | c.7797G>A | p.Leu2599Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7963/13097 | 7797/12735 | 2599/4244 | chr6 | 32058086 | |||
chr6:32058203 | G | A | 12 | a0006c0006 a0006c0045 a0012c0015 others(9): Show |
31 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(28): Show |
synonymous_variant | LOW | c.7680C>T | p.Asp2560Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7846/13097 | 7680/12735 | 2560/4244 | chr6 | 32058203 | |||
chr6:32061428 | G | A | 1 | a0016c0025 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
synonymous_variant | LOW | c.7461C>T | p.Arg2487Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7627/13097 | 7461/12735 | 2487/4244 | chr6 | 32061428 | |||
chr6:32061449 | A | G | 71 | a0001c0001 a0001c0007 a0001c0034 others(68): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
synonymous_variant | LOW | c.7440T>C | p.Tyr2480Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7606/13097 | 7440/12735 | 2480/4244 | chr6 | 32061449 | |||
chr6:32061476 | A | G | 1 | a0020c0026 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.7413T>C | p.Pro2471Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7579/13097 | 7413/12735 | 2471/4244 | chr6 | 32061476 | |||
chr6:32061512 | G | A | 4 | a0009c0029 a0027c0035 a0071c0115 others(1): Show |
9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
synonymous_variant | LOW | c.7377C>T | p.Gly2459Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7543/13097 | 7377/12735 | 2459/4244 | chr6 | 32061512 | |||
chr6:32061518 | A | G | 1 | a0019c0022 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.7371T>C | p.Val2457Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7537/13097 | 7371/12735 | 2457/4244 | chr6 | 32061518 | |||
chr6:32061638 | T | C | 64 | a0001c0001 a0001c0007 a0001c0034 others(61): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): Show |
synonymous_variant | LOW | c.7251A>G | p.Leu2417Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7417/13097 | 7251/12735 | 2417/4244 | chr6 | 32061638 | |||
chr6:32062200 | G | A | 1 | a0020c0058 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.7125C>T | p.His2375His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7291/13097 | 7125/12735 | 2375/4244 | chr6 | 32062200 | |||
chr6:32064912 | C | T | 3 | a0057c0122 a0073c0123 a0093c0119 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.6750G>A | p.Ser2250Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6916/13097 | 6750/12735 | 2250/4244 | chr6 | 32064912 | |||
chr6:32064966 | G | A | 39 | a0001c0001 a0001c0007 a0001c0034 others(36): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
synonymous_variant | LOW | c.6696C>T | p.Asp2232Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6862/13097 | 6696/12735 | 2232/4244 | chr6 | 32064966 | |||
chr6:32067692 | G | A | 5 | a0005c0013 a0005c0023 a0005c0024 others(2): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.6513C>T | p.Arg2171Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6679/13097 | 6513/12735 | 2171/4244 | chr6 | 32067692 | |||
chr6:32067857 | G | A | 9 | a0002c0095 a0005c0013 a0005c0023 others(6): Show |
23 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(20): Show |
synonymous_variant | LOW | c.6348C>T | p.Thr2116Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6514/13097 | 6348/12735 | 2116/4244 | chr6 | 32067857 | |||
chr6:32067917 | C | T | 1 | a0016c0025 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
synonymous_variant | LOW | c.6288G>A | p.Pro2096Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6454/13097 | 6288/12735 | 2096/4244 | chr6 | 32067917 | |||
chr6:32067929 | G | A | 1 | a0002c0096 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.6276C>T | p.Pro2092Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6442/13097 | 6276/12735 | 2092/4244 | chr6 | 32067929 | |||
chr6:32068580 | G | A | 21 | a0004c0008 a0004c0011 a0004c0061 others(18): Show |
71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
synonymous_variant | LOW | c.6030C>T | p.Pro2010Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6196/13097 | 6030/12735 | 2010/4244 | chr6 | 32068580 | |||
chr6:32068586 | T | C | 1 | a0019c0022 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.6024A>G | p.Thr2008Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6190/13097 | 6024/12735 | 2008/4244 | chr6 | 32068586 | |||
chr6:32068673 | G | A | 5 | a0005c0013 a0005c0023 a0005c0024 others(2): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.5937C>T | p.Thr1979Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6103/13097 | 5937/12735 | 1979/4244 | chr6 | 32068673 | |||
chr6:32068901 | G | A | 2 | a0004c0008 a0081c0062 |
11 | HG00741.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
synonymous_variant | LOW | c.5823C>T | p.Ser1941Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5989/13097 | 5823/12735 | 1941/4244 | chr6 | 32068901 | |||
chr6:32069045 | C | T | 1 | a0087c0124 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.5679G>A | p.Thr1893Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5845/13097 | 5679/12735 | 1893/4244 | chr6 | 32069045 | |||
chr6:32070206 | G | C | 1 | a0003c0113 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.5199C>G | p.Ala1733Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/44 | 5365/13097 | 5199/12735 | 1733/4244 | chr6 | 32070206 | |||
chr6:32079055 | C | T | 3 | a0057c0122 a0073c0123 a0093c0119 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.4353G>A | p.Pro1451Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4519/13097 | 4353/12735 | 1451/4244 | chr6 | 32079055 | |||
chr6:32079076 | G | A | 3 | a0002c0042 a0035c0043 a0049c0055 |
5 | HG01361.hp2 HG02145.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.4332C>T | p.His1444His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4498/13097 | 4332/12735 | 1444/4244 | chr6 | 32079076 | |||
chr6:32079289 | C | T | 1 | a0012c0098 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.4119G>A | p.Pro1373Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4285/13097 | 4119/12735 | 1373/4244 | chr6 | 32079289 | |||
chr6:32081600 | G | A | 1 | a0028c0068 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.3810C>T | p.Thr1270Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3976/13097 | 3810/12735 | 1270/4244 | chr6 | 32081600 | |||
chr6:32081645 | G | C | 1 | a0090c0073 | 1 | NA19081.hp2 | synonymous_variant | LOW | c.3765C>G | p.Arg1255Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3931/13097 | 3765/12735 | 1255/4244 | chr6 | 32081645 | |||
chr6:32084450 | C | T | 1 | a0088c0072 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.3408G>A | p.Lys1136Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3574/13097 | 3408/12735 | 1136/4244 | chr6 | 32084450 | |||
chr6:32089353 | T | C | 1 | a0062c0117 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2385A>G | p.Thr795Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2551/13097 | 2385/12735 | 795/4244 | chr6 | 32089353 | |||
chr6:32089365 | G | A | 2 | a0024c0052 a0024c0125 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.2373C>T | p.Ser791Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2539/13097 | 2373/12735 | 791/4244 | chr6 | 32089365 | |||
chr6:32089371 | C | T | 1 | a0008c0005 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
synonymous_variant | LOW | c.2367G>A | p.Gly789Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2533/13097 | 2367/12735 | 789/4244 | chr6 | 32089371 | |||
chr6:32095831 | G | T | 1 | a0009c0069 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.2022C>A | p.Gly674Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2188/13097 | 2022/12735 | 674/4244 | chr6 | 32095831 | |||
chr6:32096119 | G | A | 1 | a0017c0017 | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1900/13097 | 1734/12735 | 578/4244 | chr6 | 32096119 | |||
chr6:32096944 | G | C | 2 | a0024c0052 a0024c0125 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.909C>G | p.Gly303Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1075/13097 | 909/12735 | 303/4244 | chr6 | 32096944 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041186 | C | T | 55 | a0001c0001t0002 a0002c0012t0002 a0002c0019t0002 others(52): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*163G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 163 | chr6 | 32041186 | ||||||
chr6:32041197 | C | A | 1 | a0003c0048t0005 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 152 | chr6 | 32041197 | ||||||
chr6:32041227 | G | A | 3 | a0057c0122t0004 a0073c0123t0004 a0093c0119t0004 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*122C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 122 | chr6 | 32041227 | ||||||
chr6:32041248 | T | C | 1 | a0014c0016t0006 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 101 | chr6 | 32041248 | ||||||
chr6:32041310 | C | T | 1 | a0017c0017t0003 | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*39G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 39 | chr6 | 32041310 | ||||||
chr6:32109327 | G | A | 1 | a0041c0071t0007 | 1 | HG00140.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/44 | chr6 | 32109327 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041502 | T | C | 48 | a0002c0002t0001g0116 a0006c0006t0001g0218 a0006c0006t0001g0311 others(45): Show |
51 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.12634-52A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041502 | |||||||
chr6:32041507 | G | A | 16 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(13): Show |
17 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.12634-57C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041507 | |||||||
chr6:32041524 | A | G | 42 | a0002c0042t0002g0081 a0002c0042t0002g0142 a0003c0003t0002g0343 others(39): Show |
44 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.12634-74T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041524 | |||||||
chr6:32041574 | C | T | 35 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(32): Show |
37 | HG00140.hp1 HG01167.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.12634-124G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041574 | |||||||
chr6:32041577 | T | C | 33 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(30): Show |
35 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.12634-127A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041577 | |||||||
chr6:32041598 | T | C | 32 | a0002c0012t0002g0082 a0002c0042t0002g0142 a0006c0006t0001g0218 others(29): Show |
34 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.12634-148A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041598 | |||||||
chr6:32041608 | C | T | 31 | a0002c0042t0002g0142 a0006c0006t0001g0218 a0006c0006t0001g0311 others(28): Show |
33 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.12634-158G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041608 | |||||||
chr6:32041630 | C | T | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.12633+141G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041630 | |||||||
chr6:32041679 | A | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.12633+92T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041679 | |||||||
chr6:32042010 | A | G | 4 | a0004c0061t0001g0176 a0023c0032t0001g0180 a0023c0032t0001g0188 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.12469+2T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 42/43 | chr6 | 32042010 | |||||||
chr6:32042239 | G | C | 51 | a0002c0002t0001g0122 a0002c0042t0002g0142 a0002c0095t0001g0134 others(48): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.12307+27C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 41/43 | chr6 | 32042239 | |||||||
chr6:32042402 | G | A | 1 | a0059c0078t0001g0371 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12211-40C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042402 | |||||||
chr6:32042412 | A | C | 52 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(49): Show |
54 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(51): Show |
intron_variant | MODIFIER | c.12210+43T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042412 | |||||||
chr6:32042415 | C | CT | 52 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(49): Show |
54 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(51): Show |
intron_variant | MODIFIER | c.12210+39dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042415 | |||||||
chr6:32042419 | C | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12210+36G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042419 | |||||||
chr6:32042450 | C | T | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.12210+5G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042450 | |||||||
chr6:32042684 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG00280.hp2 HG01123.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.12058+15G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/43 | chr6 | 32042684 | |||||||
chr6:32042688 | C | T | 1 | a0001c0034t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12058+11G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/43 | chr6 | 32042688 | |||||||
chr6:32042848 | G | C | 1 | a0017c0017t0003g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.11926-17C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/43 | chr6 | 32042848 | |||||||
chr6:32042945 | G | C | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.11925+6C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/43 | chr6 | 32042945 | |||||||
chr6:32043345 | G | C | 1 | a0002c0002t0001g0130 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.11651-27C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/43 | chr6 | 32043345 | |||||||
chr6:32043427 | G | C | 159 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(156): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.11650+10C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/43 | chr6 | 32043427 | |||||||
chr6:32043581 | A | G | 199 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(196): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.11531-25T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043581 | |||||||
chr6:32043591 | C | T | 4 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 others(1): Show |
4 | HG02738.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.11531-35G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043591 | |||||||
chr6:32043592 | G | T | 78 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(75): Show |
85 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.11531-36C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043592 | |||||||
chr6:32043644 | C | T | 23 | a0001c0001t0001g0257 a0002c0002t0001g0113 a0003c0048t0002g0352 others(20): Show |
23 | HG00438.hp1 HG01123.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.11531-88G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043644 | |||||||
chr6:32043693 | C | G | 21 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(18): Show |
21 | HG01952.hp1 HG02027.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.11530+56G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043693 | |||||||
chr6:32043703 | G | A | 1 | a0082c0108t0002g0364 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.11530+46C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043703 | |||||||
chr6:32043711 | G | C | 1 | a0067c0060t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.11530+38C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043711 | |||||||
chr6:32043712 | G | A | 1 | a0082c0108t0002g0364 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.11530+37C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043712 | |||||||
chr6:32043911 | G | A | 1 | a0038c0047t0002g0353 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.11387-19C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043911 | |||||||
chr6:32043936 | C | T | 2 | a0004c0011t0001g0182 a0004c0011t0001g0184 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.11387-44G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043936 | |||||||
chr6:32043937 | A | G | 184 | a0001c0007t0001g0304 a0002c0012t0002g0082 a0002c0096t0002g0044 others(181): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.11387-45T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043937 | |||||||
chr6:32043959 | A | T | 1 | a0056c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.11386+48T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043959 | |||||||
chr6:32043992 | T | C | 3 | a0003c0003t0002g0242 a0003c0003t0002g0249 a0003c0003t0002g0307 |
3 | NA18612.hp2 NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.11386+15A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043992 | |||||||
chr6:32044149 | C | T | 4 | a0012c0015t0001g0320 a0012c0015t0001g0324 a0076c0064t0001g0338 others(1): Show |
4 | HG03834.hp1 NA18948.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.11264-20G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044149 | |||||||
chr6:32044177 | T | C | 138 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0107 others(135): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.11264-48A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044177 | |||||||
chr6:32044184 | A | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0107 others(156): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.11264-55T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044184 | |||||||
chr6:32044223 | C | T | 11 | a0003c0003t0002g0345 a0003c0003t0002g0346 a0003c0003t0002g0354 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.11264-94G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044223 | |||||||
chr6:32044250 | T | C | 1 | a0021c0027t0001g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11264-121A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044250 | |||||||
chr6:32044342 | A | G | 51 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(48): Show |
58 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.11263+39T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044342 | |||||||
chr6:32044732 | G | A | 2 | a0033c0049t0002g0245 a0033c0049t0002g0246 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.10928-16C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044732 | |||||||
chr6:32044780 | G | A | 1 | a0002c0040t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.10928-64C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044780 | |||||||
chr6:32044810 | C | T | 41 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(38): Show |
45 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.10928-94G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044810 | |||||||
chr6:32045352 | A | G | 1 | a0057c0122t0004g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10607-26T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045352 | |||||||
chr6:32045503 | G | A | 3 | a0030c0030t0001g0168 a0030c0030t0001g0169 a0030c0030t0001g0170 |
3 | NA18977.hp1 NA19004.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.10607-177C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045503 | |||||||
chr6:32045582 | C | T | 1 | a0001c0034t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.10607-256G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045582 | |||||||
chr6:32045680 | C | T | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.10607-354G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045680 | |||||||
chr6:32045723 | T | C | 74 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(71): Show |
81 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.10607-397A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045723 | |||||||
chr6:32045777 | C | T | 2 | a0061c0076t0002g0049 a0091c0067t0002g0203 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.10606+398G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045777 | |||||||
chr6:32045850 | G | A | 1 | a0006c0045t0001g0329 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10606+325C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045850 | |||||||
chr6:32045859 | A | G | 1 | a0056c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10606+316T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045859 | |||||||
chr6:32045863 | G | T | 7 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 others(4): Show |
8 | HG02083.hp2 HG02155.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.10606+312C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045863 | |||||||
chr6:32045892 | C | A | 1 | a0084c0086t0001g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.10606+283G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045892 | |||||||
chr6:32045905 | A | G | 1 | a0065c0085t0002g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10606+270T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045905 | |||||||
chr6:32045913 | T | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(76): Show |
83 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.10606+262A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045913 | |||||||
chr6:32045922 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.10606+253G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045922 | |||||||
chr6:32045981 | T | A | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.10606+194A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045981 | |||||||
chr6:32046679 | C | T | 34 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(31): Show |
36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.10325-223G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046679 | |||||||
chr6:32046798 | A | G | 230 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.10325-342T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046798 | |||||||
chr6:32046969 | C | T | 1 | a0084c0086t0001g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.10325-513G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046969 | |||||||
chr6:32047051 | G | A | 5 | a0016c0025t0002g0052 a0016c0025t0002g0087 a0016c0025t0002g0088 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.10325-595C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047051 | |||||||
chr6:32047058 | G | A | 1 | a0038c0047t0002g0353 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.10325-602C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047058 | |||||||
chr6:32047180 | C | A | 1 | a0063c0099t0001g0313 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.10324+554G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047180 | |||||||
chr6:32047265 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.10324+469C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047265 | |||||||
chr6:32047549 | C | T | 1 | a0056c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10324+185G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047549 | |||||||
chr6:32047651 | C | T | 38 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(35): Show |
38 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.10324+83G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047651 | |||||||
chr6:32048019 | A | G | 57 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(54): Show |
57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.10046-7T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048019 | |||||||
chr6:32048087 | C | T | 13 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(10): Show |
13 | HG00438.hp1 HG02027.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.10046-75G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048087 | |||||||
chr6:32048109 | C | T | 1 | a0009c0029t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.10046-97G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048109 | |||||||
chr6:32048320 | G | T | 1 | a0006c0045t0001g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10045+43C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048320 | |||||||
chr6:32048743 | C | T | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.9758-93G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048743 | |||||||
chr6:32048748 | T | G | 1 | a0001c0001t0002g0265 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.9758-98A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048748 | |||||||
chr6:32048891 | G | C | 9 | a0009c0029t0001g0055 a0009c0029t0001g0073 a0009c0029t0001g0074 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.9758-241C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048891 | |||||||
chr6:32049225 | G | C | 1 | a0001c0001t0001g0298 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.9757+45C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32049225 | |||||||
chr6:32049258 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.9757+12G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32049258 | |||||||
chr6:32049596 | GAGA | G | 6 | a0015c0014t0001g0286 a0015c0014t0001g0287 a0015c0014t0001g0295 others(3): Show |
6 | HG02293.hp2 NA18956.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.9440-12_9440-10del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049596 | |||||||
chr6:32049744 | C | T | 36 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(33): Show |
43 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.9440-157G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049744 | |||||||
chr6:32049745 | G | A | 5 | a0017c0017t0003g0205 a0017c0017t0003g0206 a0017c0017t0003g0207 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9440-158C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049745 | |||||||
chr6:32049747 | A | G | 5 | a0017c0017t0003g0205 a0017c0017t0003g0206 a0017c0017t0003g0207 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9440-160T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049747 | |||||||
chr6:32049763 | A | G | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.9440-176T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049763 | |||||||
chr6:32049768 | T | TG | 13 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(10): Show |
14 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.9440-182dupC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049768 | |||||||
chr6:32049830 | G | C | 4 | a0002c0040t0002g0094 a0039c0038t0002g0095 a0039c0038t0002g0096 others(1): Show |
4 | HG00741.hp1 HG03704.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.9439+168C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049830 | |||||||
chr6:32049839 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.9439+159C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049839 | |||||||
chr6:32050410 | A | G | 1 | a0003c0003t0001g0342 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.9116-89T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050410 | |||||||
chr6:32050426 | C | A | 1 | a0061c0076t0002g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.9116-105G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050426 | |||||||
chr6:32050462 | C | T | 20 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(17): Show |
20 | HG00438.hp1 HG00735.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.9116-141G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050462 | |||||||
chr6:32050517 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.9116-196T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050517 | |||||||
chr6:32050568 | C | G | 5 | a0017c0017t0003g0205 a0017c0017t0003g0206 a0017c0017t0003g0207 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9116-247G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050568 | |||||||
chr6:32050592 | T | C | 2 | a0001c0007t0001g0304 a0044c0089t0001g0136 |
2 | HG00673.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.9116-271A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050592 | |||||||
chr6:32050633 | G | A | 10 | a0007c0004t0001g0001 a0007c0004t0001g0185 a0007c0004t0001g0193 others(7): Show |
14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.9116-312C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050633 | |||||||
chr6:32050694 | G | A | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.9116-373C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050694 | |||||||
chr6:32050796 | A | C | 34 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(31): Show |
36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.9116-475T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050796 | |||||||
chr6:32051094 | C | T | 1 | a0082c0108t0002g0364 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.9116-773G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051094 | |||||||
chr6:32051419 | G | C | 1 | a0001c0001t0001g0288 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9116-1098C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051419 | |||||||
chr6:32051458 | A | C | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.9116-1137T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051458 | |||||||
chr6:32051605 | A | C | 1 | a0001c0034t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.9115+1065T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051605 | |||||||
chr6:32051735 | T | C | 7 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0315 others(4): Show |
7 | HG00140.hp1 HG02080.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.9115+935A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051735 | |||||||
chr6:32051969 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.9115+701C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051969 | |||||||
chr6:32051992 | G | A | 59 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(56): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.9115+678C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051992 | |||||||
chr6:32052070 | T | C | 6 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.9115+600A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052070 | |||||||
chr6:32052169 | C | T | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.9115+501G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052169 | |||||||
chr6:32052204 | C | A | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.9115+466G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052204 | |||||||
chr6:32052237 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9115+433C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052237 | |||||||
chr6:32052450 | C | CA | 20 | a0001c0001t0001g0111 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
22 | HG00140.hp1 HG02080.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.9115+219dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052450 | |||||||
chr6:32052450 | CA | C | 10 | a0001c0001t0001g0266 a0001c0001t0001g0289 a0001c0007t0001g0276 others(7): Show |
10 | HG01934.hp1 HG01975.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.9115+219delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052450 | |||||||
chr6:32052461 | A | G | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.9115+209T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052461 | |||||||
chr6:32052557 | T | C | 1 | a0075c0056t0001g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.9115+113A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052557 | |||||||
chr6:32053067 | G | A | 28 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(25): Show |
30 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.8792-74C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053067 | |||||||
chr6:32053333 | G | C | 1 | a0091c0067t0002g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8791+55C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053333 | |||||||
chr6:32053353 | C | T | 22 | a0009c0020t0001g0051 a0009c0020t0001g0075 a0009c0020t0001g0076 others(19): Show |
22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8791+35G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053353 | |||||||
chr6:32053852 | T | C | 1 | a0067c0060t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8468-141A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053852 | |||||||
chr6:32053885 | C | T | 21 | a0009c0020t0001g0051 a0009c0020t0001g0075 a0009c0020t0001g0076 others(18): Show |
21 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.8468-174G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053885 | |||||||
chr6:32053913 | A | C | 5 | a0004c0011t0001g0190 a0004c0061t0001g0176 a0023c0032t0001g0180 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.8468-202T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053913 | |||||||
chr6:32053999 | G | C | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.8468-288C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053999 | |||||||
chr6:32054061 | A | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.8468-350T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054061 | |||||||
chr6:32054075 | A | G | 37 | a0004c0011t0001g0162 a0004c0011t0001g0182 a0004c0011t0001g0183 others(34): Show |
39 | HG00558.hp1 HG00738.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.8468-364T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054075 | |||||||
chr6:32054182 | C | T | 1 | a0006c0006t0001g0218 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.8468-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054182 | |||||||
chr6:32054185 | C | G | 6 | a0005c0024t0001g0219 a0005c0024t0001g0220 a0005c0024t0001g0221 others(3): Show |
6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.8468-474G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054185 | |||||||
chr6:32054199 | A | G | 22 | a0009c0020t0001g0051 a0009c0020t0001g0075 a0009c0020t0001g0076 others(19): Show |
22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8468-488T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054199 | |||||||
chr6:32054212 | GC | G | 2 | a0021c0027t0001g0008 a0021c0027t0001g0174 |
4 | HG02129.hp2 HG03471.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.8468-502delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054212 | |||||||
chr6:32054370 | A | G | 15 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(12): Show |
17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.8468-659T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054370 | |||||||
chr6:32054852 | A | G | 1 | a0091c0067t0002g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8467+999T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054852 | |||||||
chr6:32054860 | C | G | 1 | a0002c0002t0001g0011 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.8467+991G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054860 | |||||||
chr6:32055056 | T | G | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.8467+795A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055056 | |||||||
chr6:32055121 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.8467+730G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055121 | |||||||
chr6:32055152 | C | T | 1 | a0001c0007t0001g0304 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.8467+699G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055152 | |||||||
chr6:32055202 | C | A | 2 | a0052c0116t0001g0370 a0059c0078t0001g0371 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.8467+649G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055202 | |||||||
chr6:32055234 | T | A | 21 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(18): Show |
23 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.8467+617A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055234 | |||||||
chr6:32055348 | C | T | 1 | a0009c0069t0001g0079 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8467+503G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055348 | |||||||
chr6:32055366 | G | A | 2 | a0009c0020t0001g0051 a0089c0090t0002g0143 |
2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.8467+485C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055366 | |||||||
chr6:32055648 | C | T | 14 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(11): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.8467+203G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055648 | |||||||
chr6:32055716 | A | G | 2 | a0031c0051t0001g0030 a0031c0051t0001g0031 |
2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.8467+135T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055716 | |||||||
chr6:32055754 | C | A | 6 | a0005c0024t0001g0219 a0005c0024t0001g0220 a0005c0024t0001g0221 others(3): Show |
6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.8467+97G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055754 | |||||||
chr6:32055766 | G | A | 2 | a0009c0020t0001g0051 a0089c0090t0002g0143 |
2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.8467+85C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055766 | |||||||
chr6:32056277 | T | A | 1 | a0001c0109t0001g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8144-103A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/43 | chr6 | 32056277 | |||||||
chr6:32056378 | T | C | 1 | a0073c0123t0004g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8144-204A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/43 | chr6 | 32056378 | |||||||
chr6:32057004 | C | T | 3 | a0002c0002t0001g0116 a0002c0002t0001g0130 a0002c0002t0001g0150 |
3 | HG02056.hp1 NA18971.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.7826-101G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057004 | |||||||
chr6:32057005 | G | A | 13 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(10): Show |
13 | HG00438.hp1 HG02027.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.7826-102C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057005 | |||||||
chr6:32057055 | T | C | 232 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(229): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.7826-152A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057055 | |||||||
chr6:32057281 | C | A | 12 | a0005c0013t0001g0228 a0005c0013t0001g0231 a0005c0013t0001g0232 others(9): Show |
12 | HG00438.hp1 HG02132.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.7826-378G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057281 | |||||||
chr6:32057379 | A | C | 1 | a0037c0041t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7826-476T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057379 | |||||||
chr6:32057524 | G | A | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7825+534C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057524 | |||||||
chr6:32057538 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.7825+520G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057538 | |||||||
chr6:32057539 | T | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.7825+519A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057539 | |||||||
chr6:32057549 | C | T | 59 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(56): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.7825+509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057549 | |||||||
chr6:32057633 | ACT | A | 34 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(31): Show |
36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.7825+423_7825+424d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057633 | |||||||
chr6:32057663 | T | C | 2 | a0052c0116t0001g0370 a0059c0078t0001g0371 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.7825+395A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057663 | |||||||
chr6:32057778 | C | A | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.7825+280G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057778 | |||||||
chr6:32058031 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.7825+27T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32058031 | |||||||
chr6:32058435 | CA | C | 14 | a0020c0026t0001g0157 a0020c0026t0001g0164 a0020c0026t0001g0167 others(11): Show |
14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.7493-46delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058435 | |||||||
chr6:32058480 | T | C | 364 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(361): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.7493-90A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058480 | |||||||
chr6:32058551 | C | T | 2 | a0047c0094t0001g0283 a0062c0117t0002g0149 |
2 | HG01346.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.7493-161G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058551 | |||||||
chr6:32058629 | CAT | C | 6 | a0025c0033t0002g0152 a0025c0033t0002g0153 a0025c0033t0002g0155 others(3): Show |
6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.7493-241_7493-240d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058629 | |||||||
chr6:32058733 | T | G | 1 | a0089c0090t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-343A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058733 | |||||||
chr6:32058736 | A | C | 1 | a0089c0090t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-346T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058736 | |||||||
chr6:32058819 | T | A | 1 | a0089c0090t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-429A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058819 | |||||||
chr6:32058873 | T | A | 1 | a0089c0090t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-483A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058873 | |||||||
chr6:32058900 | G | A | 1 | a0004c0008t0001g0014 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7493-510C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058900 | |||||||
chr6:32059031 | G | A | 29 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(26): Show |
31 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.7493-641C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059031 | |||||||
chr6:32059032 | G | C | 1 | a0020c0026t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7493-642C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059032 | |||||||
chr6:32059131 | A | G | 1 | a0073c0123t0004g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7493-741T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059131 | |||||||
chr6:32059418 | C | CA | 61 | a0001c0001t0001g0241 a0001c0001t0001g0267 a0002c0002t0001g0007 others(58): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.7493-1029dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059418 | |||||||
chr6:32059418 | CA | C | 20 | a0001c0001t0001g0005 a0001c0007t0001g0278 a0002c0002t0001g0125 others(17): Show |
22 | NA18612.hp1 NA18945.hp2 NA18950.hp1 others(19): Show |
intron_variant | MODIFIER | c.7493-1029delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059418 | |||||||
chr6:32059669 | A | T | 5 | a0006c0006t0001g0312 a0006c0006t0001g0314 a0006c0006t0001g0330 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.7493-1279T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059669 | |||||||
chr6:32059784 | T | C | 1 | a0070c0079t0001g0372 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7493-1394A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059784 | |||||||
chr6:32059889 | C | T | 1 | a0020c0058t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.7493-1499G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059889 | |||||||
chr6:32059983 | T | C | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7492+1414A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059983 | |||||||
chr6:32060105 | C | T | 1 | a0005c0013t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.7492+1292G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060105 | |||||||
chr6:32060300 | C | CCAGCCTG others(62): Show |
1 | a0020c0026t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7492+1096_7492+109 others(73): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060300 | |||||||
chr6:32060300 | C | CCAGCCTG others(61): Show |
13 | a0020c0026t0001g0157 a0020c0026t0001g0164 a0020c0026t0001g0172 others(10): Show |
13 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.7492+1029_7492+109 others(72): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060300 | |||||||
chr6:32060332 | C | CA | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.7492+1064dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060332 | |||||||
chr6:32060332 | CA | C | 14 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(11): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.7492+1064delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060332 | |||||||
chr6:32060372 | G | C | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.7492+1025C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060372 | |||||||
chr6:32060420 | TATATATT others(18): Show |
T | 1 | a0086c0084t0001g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7492+952_7492+976d others(27): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060420 | |||||||
chr6:32060644 | T | C | 1 | a0047c0094t0001g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.7492+753A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060644 | |||||||
chr6:32060732 | G | A | 1 | a0001c0034t0001g0262 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.7492+665C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060732 | |||||||
chr6:32061173 | T | C | 2 | a0004c0011t0001g0182 a0004c0011t0001g0184 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7492+224A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061173 | |||||||
chr6:32061228 | C | G | 2 | a0010c0087t0002g0046 a0069c0065t0002g0175 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.7492+169G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061228 | |||||||
chr6:32061247 | C | T | 2 | a0029c0031t0001g0204 a0062c0117t0002g0149 |
2 | HG02615.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.7492+150G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061247 | |||||||
chr6:32061283 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7492+114C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061283 | |||||||
chr6:32061389 | C | T | 3 | a0009c0020t0001g0075 a0009c0020t0001g0076 a0009c0020t0001g0077 |
3 | HG00597.hp2 HG02132.hp2 NA18951.hp2 |
splice_region_variant&intron_variant | LOW | c.7492+8G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061389 | |||||||
chr6:32061751 | G | A | 1 | a0003c0003t0002g0360 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7169-31C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061751 | |||||||
chr6:32061968 | A | G | 4 | a0001c0001t0001g0301 a0009c0020t0001g0075 a0009c0020t0001g0076 others(1): Show |
4 | HG00597.hp2 HG02056.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.7168+189T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061968 | |||||||
chr6:32061969 | T | C | 2 | a0057c0122t0004g0226 a0073c0123t0004g0225 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7168+188A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061969 | |||||||
chr6:32061992 | G | A | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7168+165C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061992 | |||||||
chr6:32062072 | G | A | 59 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(56): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.7168+85C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062072 | |||||||
chr6:32062138 | G | T | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.7168+19C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062138 | |||||||
chr6:32062146 | C | T | 1 | a0020c0026t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7168+11G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062146 | |||||||
chr6:32062152 | C | T | 10 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(7): Show |
11 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.7168+5G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062152 | |||||||
chr6:32062507 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.6842-24C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062507 | |||||||
chr6:32062712 | G | C | 1 | a0002c0002t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6842-229C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062712 | |||||||
chr6:32062923 | C | T | 8 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(5): Show |
10 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6842-440G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062923 | |||||||
chr6:32063045 | T | C | 1 | a0003c0003t0002g0366 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6842-562A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063045 | |||||||
chr6:32063047 | C | T | 9 | a0012c0015t0001g0320 a0012c0015t0001g0321 a0012c0015t0001g0323 others(6): Show |
10 | HG02622.hp1 HG02735.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.6842-564G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063047 | |||||||
chr6:32063142 | C | G | 1 | a0020c0026t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6842-659G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063142 | |||||||
chr6:32063197 | G | C | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6842-714C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063197 | |||||||
chr6:32063404 | G | GA | 19 | a0001c0001t0001g0291 a0005c0013t0001g0045 a0005c0013t0001g0228 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6842-922dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063404 | |||||||
chr6:32063404 | GA | G | 26 | a0001c0007t0001g0278 a0010c0010t0001g0022 a0010c0010t0002g0009 others(23): Show |
28 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.6842-922delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063404 | |||||||
chr6:32063479 | G | A | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6842-996C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063479 | |||||||
chr6:32063534 | T | C | 2 | a0001c0001t0002g0265 a0078c0106t0002g0269 |
2 | HG00099.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6842-1051A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063534 | |||||||
chr6:32064127 | G | A | 14 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(11): Show |
14 | HG00140.hp1 HG01884.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.6841+694C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064127 | |||||||
chr6:32064140 | G | C | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6841+681C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064140 | |||||||
chr6:32064235 | C | T | 1 | a0083c0112t0002g0341 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6841+586G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064235 | |||||||
chr6:32064238 | G | C | 1 | a0003c0048t0002g0352 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6841+583C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064238 | |||||||
chr6:32064324 | C | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6841+497G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064324 | |||||||
chr6:32064362 | G | A | 34 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(31): Show |
36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.6841+459C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064362 | |||||||
chr6:32064426 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6841+395G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064426 | |||||||
chr6:32064428 | G | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.6841+393C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064428 | |||||||
chr6:32064434 | G | T | 3 | a0026c0036t0002g0012 a0026c0053t0002g0161 a0056c0054t0002g0158 |
4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.6841+387C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064434 | |||||||
chr6:32064529 | C | T | 59 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(56): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.6841+292G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064529 | |||||||
chr6:32064572 | C | T | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6841+249G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064572 | |||||||
chr6:32064644 | C | T | 65 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(62): Show |
72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.6841+177G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064644 | |||||||
chr6:32065230 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.6545-113C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065230 | |||||||
chr6:32065674 | C | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6545-557G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065674 | |||||||
chr6:32065682 | C | T | 1 | a0012c0015t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6545-565G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065682 | |||||||
chr6:32065770 | G | A | 2 | a0009c0020t0001g0078 a0087c0124t0002g0071 |
2 | NA19007.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6545-653C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065770 | |||||||
chr6:32065839 | G | A | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.6545-722C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065839 | |||||||
chr6:32065852 | G | C | 1 | a0002c0002t0001g0011 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6545-735C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065852 | |||||||
chr6:32066167 | A | G | 342 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(339): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.6545-1050T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066167 | |||||||
chr6:32066292 | G | C | 1 | a0012c0015t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6545-1175C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066292 | |||||||
chr6:32066315 | G | C | 2 | a0003c0048t0002g0352 a0003c0048t0005g0362 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6545-1198C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066315 | |||||||
chr6:32066399 | A | AAATC | 24 | a0002c0019t0002g0003 a0002c0019t0002g0064 a0002c0019t0002g0065 others(21): Show |
26 | HG00423.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.6544+1258_6544+126 others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066399 | |||||||
chr6:32066399 | AAATC | A | 6 | a0001c0001t0001g0255 a0002c0002t0001g0115 a0021c0027t0001g0008 others(3): Show |
8 | HG01255.hp2 HG02071.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.6544+1258_6544+126 others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066399 | |||||||
chr6:32066629 | A | G | 1 | a0020c0026t0001g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6544+1032T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066629 | |||||||
chr6:32067074 | TAAAAAGA others(6): Show |
T | 3 | a0026c0036t0002g0012 a0026c0053t0002g0161 a0056c0054t0002g0158 |
4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.6544+574_6544+586d others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067074 | |||||||
chr6:32067084 | G | GAAAGA | 248 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.6544+572_6544+576d others(7): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067084 | |||||||
chr6:32067094 | AATGAAAG | A | 3 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+560_6544+566d others(9): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067094 | |||||||
chr6:32067108 | A | T | 3 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+553T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067108 | |||||||
chr6:32067111 | AAG | A | 3 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+548_6544+549d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067111 | |||||||
chr6:32067124 | A | AAAGG | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0034t0001g0262 |
3 | HG01169.hp2 NA18961.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.6544+533_6544+536d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067124 | |||||||
chr6:32067124 | A | G | 9 | a0002c0019t0002g0003 a0002c0019t0002g0064 a0002c0019t0002g0065 others(6): Show |
11 | HG00735.hp2 HG01255.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+537T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067124 | |||||||
chr6:32067127 | GGAAGGA | G | 3 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+533d others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067127 | |||||||
chr6:32067128 | G | GAAGAAGA others(4): Show |
1 | a0040c0039t0002g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.6544+532_6544+533i others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | |||||||
chr6:32067128 | G | GAAGAAGA others(3): Show |
1 | a0012c0098t0001g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6544+532_6544+533i others(12): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | |||||||
chr6:32067128 | G | GAAGAAGA others(15): Show |
1 | a0002c0002t0001g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6544+532_6544+533i others(24): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | |||||||
chr6:32067132 | G | A | 4 | a0001c0007t0001g0281 a0002c0002t0001g0113 a0012c0098t0001g0325 others(1): Show |
4 | HG03209.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.6544+529C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGA | 36 | a0001c0001t0001g0036 a0001c0001t0001g0255 a0001c0001t0001g0288 others(33): Show |
37 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.6544+525_6544+528d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(1): Show |
48 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0224 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.6544+521_6544+528d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(5): Show |
66 | a0001c0001t0001g0015 a0001c0001t0001g0156 a0001c0001t0001g0159 others(63): Show |
70 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.6544+517_6544+528d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(9): Show |
29 | a0001c0001t0001g0160 a0002c0002t0001g0006 a0002c0002t0001g0007 others(26): Show |
32 | HG00423.hp1 HG00738.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.6544+513_6544+528d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(13): Show |
12 | a0001c0001t0001g0294 a0002c0002t0001g0006 a0002c0002t0001g0121 others(9): Show |
12 | HG00597.hp2 HG01517.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6544+509_6544+528d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(17): Show |
4 | a0003c0003t0002g0053 a0003c0003t0002g0354 a0014c0016t0002g0349 others(1): Show |
4 | HG00438.hp2 NA18972.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.6544+505_6544+528d others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAAG others(21): Show |
2 | a0002c0002t0001g0120 a0037c0041t0001g0146 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6544+501_6544+528d others(30): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGAAGA others(12): Show |
1 | a0038c0047t0002g0353 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(21): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(1): Show |
9 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0112 others(6): Show |
9 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(5): Show |
9 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0109 others(6): Show |
9 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(9): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0010c0010t0002g0009 others(7): Show |
11 | HG01074.hp1 HG01099.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(13): Show |
3 | a0001c0001t0001g0107 a0002c0040t0002g0094 a0036c0046t0001g0260 |
3 | HG00741.hp1 HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(17): Show |
1 | a0068c0097t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(21): Show |
2 | a0010c0010t0002g0034 a0034c0044t0001g0017 |
2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(30): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(5): Show |
2 | a0057c0122t0004g0226 a0073c0123t0004g0225 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAAGGAAG others(17): Show |
1 | a0093c0119t0004g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAGAAAGA others(4): Show |
1 | a0014c0016t0002g0348 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.6544+528_6544+529i others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | G | GAGAAGAA others(3): Show |
1 | a0001c0001t0001g0016 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(12): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | GAAGA | G | 6 | a0001c0007t0001g0276 a0006c0006t0001g0312 a0006c0006t0001g0314 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.6544+525_6544+528d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | GAAGAAAG others(1): Show |
G | 33 | a0005c0013t0001g0045 a0005c0024t0001g0219 a0005c0024t0001g0220 others(30): Show |
36 | HG00140.hp1 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.6544+521_6544+528d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | GAAGAAAG others(5): Show |
G | 17 | a0005c0013t0001g0228 a0005c0013t0001g0231 a0005c0013t0001g0232 others(14): Show |
17 | HG00438.hp1 HG00738.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.6544+517_6544+528d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067132 | GAAGAAAG others(9): Show |
G | 14 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(11): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.6544+513_6544+528d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | |||||||
chr6:32067140 | A | G | 1 | a0001c0007t0001g0276 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6544+521T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067140 | |||||||
chr6:32067143 | G | GAA | 10 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(7): Show |
11 | HG00741.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+516_6544+517d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067143 | |||||||
chr6:32067144 | A | G | 7 | a0005c0013t0001g0045 a0005c0024t0001g0219 a0005c0024t0001g0220 others(4): Show |
7 | HG01952.hp1 HG02027.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.6544+517T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067144 | |||||||
chr6:32067145 | AAG | A | 25 | a0004c0008t0001g0309 a0004c0011t0001g0162 a0004c0011t0001g0178 others(22): Show |
29 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.6544+514_6544+515d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067145 | |||||||
chr6:32067148 | A | G | 15 | a0005c0013t0001g0228 a0005c0013t0001g0231 a0005c0013t0001g0232 others(12): Show |
15 | HG00438.hp1 HG02132.hp1 HG03491.hp1 others(12): Show |
intron_variant | MODIFIER | c.6544+513T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067148 | |||||||
chr6:32067152 | A | AAAGAAAG others(8): Show |
1 | a0002c0093t0001g0129 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6544+494_6544+508d others(17): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067152 | |||||||
chr6:32067152 | A | G | 3 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+509T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067152 | |||||||
chr6:32067163 | G | GAAAGAAA others(9): Show |
1 | a0009c0029t0001g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6544+497_6544+498i others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067163 | |||||||
chr6:32067381 | AAG | A | 9 | a0009c0029t0001g0055 a0009c0029t0001g0073 a0009c0029t0001g0074 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.6544+278_6544+279d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067381 | |||||||
chr6:32067482 | C | T | 1 | a0010c0010t0002g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6544+179G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067482 | |||||||
chr6:32067650 | T | C | 63 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(60): Show |
71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.6544+11A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067650 | |||||||
chr6:32067653 | A | T | 3 | a0001c0001t0001g0247 a0033c0049t0002g0245 a0033c0049t0002g0246 |
3 | HG00639.hp2 HG01515.hp2 HG01517.hp2 |
splice_region_variant&intron_variant | LOW | c.6544+8T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067653 | |||||||
chr6:32068084 | A | G | 12 | a0003c0003t0002g0345 a0003c0003t0002g0346 a0003c0003t0002g0356 others(9): Show |
12 | HG00423.hp1 HG02040.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.6221-100T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068084 | |||||||
chr6:32068300 | C | A | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6220+90G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068300 | |||||||
chr6:32068335 | G | A | 1 | a0005c0024t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6220+55C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068335 | |||||||
chr6:32068358 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6220+32G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068358 | |||||||
chr6:32068753 | C | T | 1 | a0012c0098t0001g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5903-46G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/43 | chr6 | 32068753 | |||||||
chr6:32069320 | C | T | 1 | a0061c0076t0002g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5588-184G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/43 | chr6 | 32069320 | |||||||
chr6:32069372 | G | A | 1 | a0019c0022t0002g0335 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5587+181C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/43 | chr6 | 32069372 | |||||||
chr6:32070003 | G | A | 1 | a0027c0035t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5278+124C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070003 | |||||||
chr6:32070023 | C | T | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5278+104G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070023 | |||||||
chr6:32070087 | G | A | 1 | a0056c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5278+40C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070087 | |||||||
chr6:32070498 | GC | G | 14 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(11): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4991-85delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070498 | |||||||
chr6:32070773 | C | T | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.4991-359G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070773 | |||||||
chr6:32070788 | C | T | 1 | a0093c0119t0004g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4991-374G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070788 | |||||||
chr6:32070818 | C | T | 1 | a0051c0104t0001g0300 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4991-404G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070818 | |||||||
chr6:32070902 | G | A | 4 | a0007c0004t0001g0195 a0007c0004t0001g0196 a0007c0004t0001g0197 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4991-488C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070902 | |||||||
chr6:32070923 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
80 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.4991-509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070923 | |||||||
chr6:32071455 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4990+535A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071455 | |||||||
chr6:32071474 | A | G | 1 | a0013c0018t0002g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4990+516T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071474 | |||||||
chr6:32071526 | C | T | 1 | a0009c0020t0001g0076 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4990+464G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071526 | |||||||
chr6:32071578 | C | CT | 150 | a0001c0001t0001g0303 a0002c0019t0002g0003 a0002c0019t0002g0064 others(147): Show |
161 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.4990+411dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071578 | |||||||
chr6:32071578 | C | CTT | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
78 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4990+410_4990+411d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071578 | |||||||
chr6:32071676 | C | G | 1 | a0096c0063t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4990+314G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071676 | |||||||
chr6:32071873 | A | G | 1 | a0005c0024t0001g0219 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4990+117T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071873 | |||||||
chr6:32072408 | T | C | 1 | a0006c0045t0001g0329 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4682-110A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072408 | |||||||
chr6:32072632 | G | A | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4682-334C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072632 | |||||||
chr6:32072707 | T | C | 22 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(19): Show |
22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.4682-409A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072707 | |||||||
chr6:32072827 | C | T | 31 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(28): Show |
32 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.4682-529G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072827 | |||||||
chr6:32072859 | G | T | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4682-561C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072859 | |||||||
chr6:32073023 | T | C | 6 | a0025c0033t0002g0152 a0025c0033t0002g0153 a0025c0033t0002g0155 others(3): Show |
6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.4681+624A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073023 | |||||||
chr6:32073102 | T | G | 2 | a0031c0051t0001g0030 a0031c0051t0001g0031 |
2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.4681+545A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073102 | |||||||
chr6:32073154 | A | G | 85 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(82): Show |
93 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.4681+493T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073154 | |||||||
chr6:32073216 | G | A | 7 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 others(4): Show |
8 | HG01243.hp1 HG02738.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.4681+431C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073216 | |||||||
chr6:32073266 | A | C | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.4681+381T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073266 | |||||||
chr6:32073293 | G | C | 1 | a0064c0074t0002g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4681+354C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073293 | |||||||
chr6:32073516 | G | A | 1 | a0009c0020t0001g0076 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4681+131C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073516 | |||||||
chr6:32073596 | G | A | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4681+51C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073596 | |||||||
chr6:32074154 | C | G | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4376-202G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074154 | |||||||
chr6:32074214 | C | T | 6 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4376-262G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074214 | |||||||
chr6:32074273 | C | T | 1 | a0006c0006t0001g0332 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4376-321G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074273 | |||||||
chr6:32074423 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.4376-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074423 | |||||||
chr6:32074458 | T | A | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4376-506A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074458 | |||||||
chr6:32074545 | T | C | 306 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(303): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.4376-593A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074545 | |||||||
chr6:32074568 | G | A | 1 | a0007c0004t0001g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4376-616C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074568 | |||||||
chr6:32074971 | C | T | 1 | a0002c0012t0002g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4376-1019G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074971 | |||||||
chr6:32075189 | C | G | 2 | a0029c0031t0001g0171 a0029c0031t0001g0204 |
2 | NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4376-1237G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075189 | |||||||
chr6:32075380 | T | C | 4 | a0010c0010t0002g0009 a0010c0010t0002g0029 a0010c0010t0002g0032 others(1): Show |
5 | HG01074.hp1 HG01099.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.4376-1428A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075380 | |||||||
chr6:32075533 | G | A | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4376-1581C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075533 | |||||||
chr6:32075879 | C | CT | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4376-1928dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075879 | |||||||
chr6:32076209 | TGCTGGTG others(5): Show |
T | 1 | a0001c0001t0001g0292 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4376-2269_4376-225 others(16): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076209 | |||||||
chr6:32076217 | G | T | 1 | a0062c0117t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4376-2265C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076217 | |||||||
chr6:32076292 | C | T | 1 | a0006c0006t0001g0315 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4376-2340G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076292 | |||||||
chr6:32076395 | G | C | 3 | a0052c0116t0001g0370 a0059c0078t0001g0371 a0070c0079t0001g0372 |
3 | HG01891.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4376-2443C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076395 | |||||||
chr6:32076538 | A | G | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4375+2495T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076538 | |||||||
chr6:32076539 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.4375+2494G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076539 | |||||||
chr6:32076784 | C | G | 1 | a0010c0010t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4375+2249G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076784 | |||||||
chr6:32077057 | G | C | 35 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(32): Show |
40 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.4375+1976C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077057 | |||||||
chr6:32077074 | C | T | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4375+1959G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077074 | |||||||
chr6:32077075 | A | G | 1 | a0014c0016t0006g0368 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4375+1958T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077075 | |||||||
chr6:32077104 | T | TGCCTGAC others(4): Show |
1 | a0083c0112t0002g0341 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4375+1918_4375+192 others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077104 | |||||||
chr6:32077449 | T | A | 17 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(14): Show |
19 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.4375+1584A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077449 | |||||||
chr6:32077518 | A | G | 3 | a0026c0036t0002g0012 a0026c0053t0002g0161 a0056c0054t0002g0158 |
4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375+1515T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077518 | |||||||
chr6:32077670 | T | G | 1 | a0007c0004t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4375+1363A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077670 | |||||||
chr6:32077797 | C | T | 1 | a0003c0003t0002g0344 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4375+1236G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077797 | |||||||
chr6:32077957 | G | A | 1 | a0020c0026t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4375+1076C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077957 | |||||||
chr6:32078071 | A | AGAGAAAG others(8): Show |
2 | a0003c0113t0002g0361 a0038c0047t0002g0353 |
2 | HG02083.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4375+961_4375+962i others(17): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078071 | |||||||
chr6:32078073 | G | A | 2 | a0003c0113t0002g0361 a0038c0047t0002g0353 |
2 | HG02083.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4375+960C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | G | GAGAA | 71 | a0001c0001t0001g0292 a0002c0002t0001g0006 a0002c0002t0001g0007 others(68): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.4375+956_4375+959d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | G | GAGAAAGA others(1): Show |
40 | a0002c0002t0001g0115 a0002c0002t0001g0124 a0002c0002t0001g0125 others(37): Show |
43 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.4375+952_4375+959d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | G | GAGAAAGA others(5): Show |
12 | a0003c0003t0002g0345 a0003c0048t0002g0352 a0006c0006t0001g0317 others(9): Show |
14 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.4375+948_4375+959d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | G | GAGAAAGA others(9): Show |
4 | a0002c0012t0002g0067 a0002c0012t0002g0068 a0006c0006t0001g0218 others(1): Show |
4 | HG02293.hp1 HG02300.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375+944_4375+959d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | G | GAGAAAGA others(13): Show |
1 | a0002c0012t0002g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4375+940_4375+959d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAA | G | 27 | a0001c0001t0001g0016 a0001c0007t0001g0281 a0001c0007t0001g0304 others(24): Show |
30 | HG00673.hp1 HG00735.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.4375+956_4375+959d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAAAGA others(1): Show |
G | 25 | a0001c0001t0001g0156 a0001c0001t0001g0224 a0001c0001t0001g0288 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.4375+952_4375+959d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAAAGA others(5): Show |
G | 31 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0111 others(28): Show |
33 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.4375+948_4375+959d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAAAGA others(9): Show |
G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0110 others(20): Show |
25 | HG00280.hp2 HG01123.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.4375+944_4375+959d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAAAGA others(13): Show |
G | 16 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0005c0013t0001g0045 others(13): Show |
16 | HG00438.hp1 HG02027.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4375+940_4375+959d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078073 | GAGAAAGA others(17): Show |
G | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4375+936_4375+959d others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | |||||||
chr6:32078075 | GAAAGAAA others(10): Show |
G | 1 | a0005c0013t0001g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4375+941_4375+957d others(19): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078075 | |||||||
chr6:32078093 | AAGAAAG | A | 3 | a0007c0004t0001g0195 a0007c0004t0001g0196 a0007c0004t0001g0197 |
3 | HG01167.hp2 HG01169.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4375+934_4375+939d others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078093 | |||||||
chr6:32078095 | G | GAA | 3 | a0004c0008t0001g0138 a0029c0031t0001g0166 a0091c0067t0002g0203 |
3 | HG03516.hp1 NA18939.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4375+936_4375+937d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078095 | |||||||
chr6:32078097 | AAG | A | 58 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0177 others(55): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.4375+934_4375+935d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078097 | |||||||
chr6:32078133 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4375+900T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078133 | |||||||
chr6:32078309 | G | A | 1 | a0075c0056t0001g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4375+724C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078309 | |||||||
chr6:32078447 | C | CA | 111 | a0001c0001t0001g0110 a0001c0001t0001g0241 a0001c0001t0001g0270 others(108): Show |
123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.4375+585dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | |||||||
chr6:32078447 | C | CAA | 17 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0093t0001g0129 others(14): Show |
17 | HG00741.hp2 HG02080.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.4375+584_4375+585d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | |||||||
chr6:32078447 | CA | C | 20 | a0001c0001t0001g0111 a0001c0001t0001g0159 a0001c0001t0001g0294 others(17): Show |
21 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.4375+585delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | |||||||
chr6:32078498 | A | C | 23 | a0009c0020t0001g0051 a0009c0020t0001g0075 a0009c0020t0001g0076 others(20): Show |
23 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.4375+535T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078498 | |||||||
chr6:32078532 | G | A | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.4375+501C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078532 | |||||||
chr6:32078565 | C | A | 14 | a0020c0026t0001g0157 a0020c0026t0001g0164 a0020c0026t0001g0167 others(11): Show |
14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.4375+468G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078565 | |||||||
chr6:32078805 | G | A | 1 | a0044c0089t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4375+228C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078805 | |||||||
chr6:32079396 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4043-31C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079396 | |||||||
chr6:32079491 | T | C | 11 | a0002c0040t0002g0094 a0013c0018t0002g0010 a0013c0018t0002g0092 others(8): Show |
12 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.4043-126A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079491 | |||||||
chr6:32079500 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.4043-135C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079500 | |||||||
chr6:32079574 | T | G | 2 | a0006c0045t0001g0328 a0006c0045t0001g0329 |
2 | HG01515.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4043-209A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079574 | |||||||
chr6:32079659 | C | G | 64 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(61): Show |
72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.4043-294G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079659 | |||||||
chr6:32079718 | C | T | 1 | a0026c0036t0002g0012 | 2 | HG02155.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.4043-353G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079718 | |||||||
chr6:32079960 | A | C | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4043-595T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079960 | |||||||
chr6:32080217 | GT | G | 361 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(358): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.4043-853delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080217 | |||||||
chr6:32080218 | T | G | 1 | a0008c0005t0002g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4043-853A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080218 | |||||||
chr6:32080367 | T | C | 1 | a0063c0099t0001g0313 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4042+1001A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080367 | |||||||
chr6:32080456 | C | G | 1 | a0008c0005t0002g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4042+912G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080456 | |||||||
chr6:32080457 | G | C | 1 | a0008c0005t0002g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4042+911C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080457 | |||||||
chr6:32080633 | G | T | 3 | a0009c0020t0001g0075 a0009c0020t0001g0076 a0009c0020t0001g0077 |
3 | HG00597.hp2 HG02132.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.4042+735C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080633 | |||||||
chr6:32080846 | T | C | 1 | a0068c0097t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4042+522A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080846 | |||||||
chr6:32080903 | G | A | 6 | a0025c0033t0002g0152 a0025c0033t0002g0153 a0025c0033t0002g0155 others(3): Show |
6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.4042+465C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080903 | |||||||
chr6:32080975 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4042+393C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080975 | |||||||
chr6:32081736 | C | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3737-63G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081736 | |||||||
chr6:32081960 | G | C | 1 | a0002c0002t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3736+76C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081960 | |||||||
chr6:32081961 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3736+75G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081961 | |||||||
chr6:32082029 | T | A | 1 | a0004c0011t0001g0198 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.3736+7A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32082029 | |||||||
chr6:32082636 | A | C | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3446-310T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082636 | |||||||
chr6:32082767 | C | T | 341 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.3446-441G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082767 | |||||||
chr6:32082844 | G | A | 2 | a0003c0048t0002g0352 a0003c0048t0005g0362 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3446-518C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082844 | |||||||
chr6:32082876 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.3446-550G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082876 | |||||||
chr6:32082981 | C | T | 18 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0013c0018t0002g0010 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.3446-655G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082981 | |||||||
chr6:32083030 | C | T | 1 | a0057c0122t0004g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3446-704G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083030 | |||||||
chr6:32083123 | C | T | 1 | a0049c0055t0002g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3446-797G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083123 | |||||||
chr6:32083420 | A | G | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3445+993T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083420 | |||||||
chr6:32083599 | C | T | 1 | a0002c0040t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3445+814G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083599 | |||||||
chr6:32083762 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3445+651G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083762 | |||||||
chr6:32083818 | G | A | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3445+595C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083818 | |||||||
chr6:32083855 | G | A | 1 | a0011c0009t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3445+558C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083855 | |||||||
chr6:32084089 | C | A | 1 | a0095c0092t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3445+324G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32084089 | |||||||
chr6:32084312 | CTCCAGGA others(5): Show |
C | 25 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(22): Show |
26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.3445+89_3445+100de others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32084312 | |||||||
chr6:32085121 | C | T | 37 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(34): Show |
44 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.3149-412G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085121 | |||||||
chr6:32085206 | C | T | 64 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(61): Show |
72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.3149-497G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085206 | |||||||
chr6:32085385 | A | G | 4 | a0001c0001t0001g0291 a0001c0001t0001g0298 a0001c0001t0001g0299 others(1): Show |
4 | NA18957.hp2 NA18973.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3148+365T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085385 | |||||||
chr6:32085425 | G | A | 4 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 others(1): Show |
4 | HG02738.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3148+325C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085425 | |||||||
chr6:32085566 | C | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3148+184G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085566 | |||||||
chr6:32085674 | C | T | 1 | a0049c0055t0002g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3148+76G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085674 | |||||||
chr6:32086435 | C | G | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-317G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086435 | |||||||
chr6:32086569 | C | A | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-451G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086569 | |||||||
chr6:32086832 | A | G | 1 | a0012c0015t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2780-714T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086832 | |||||||
chr6:32086882 | C | T | 3 | a0011c0009t0002g0057 a0011c0009t0002g0059 a0011c0009t0002g0061 |
3 | HG02080.hp2 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2780-764G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086882 | |||||||
chr6:32086938 | A | G | 1 | a0085c0059t0001g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2780-820T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086938 | |||||||
chr6:32086965 | T | G | 1 | a0002c0040t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2780-847A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086965 | |||||||
chr6:32087089 | T | C | 1 | a0013c0018t0002g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2780-971A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087089 | |||||||
chr6:32087107 | G | C | 15 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(12): Show |
17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.2780-989C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087107 | |||||||
chr6:32087157 | G | A | 32 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(29): Show |
37 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-1039C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087157 | |||||||
chr6:32087210 | T | C | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2780-1092A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087210 | |||||||
chr6:32087609 | G | A | 1 | a0026c0053t0002g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2779+1176C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087609 | |||||||
chr6:32087824 | G | T | 1 | a0074c0082t0002g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2779+961C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087824 | |||||||
chr6:32087922 | G | T | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2779+863C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087922 | |||||||
chr6:32088018 | A | C | 1 | a0002c0002t0001g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2779+767T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088018 | |||||||
chr6:32088165 | C | G | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2779+620G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088165 | |||||||
chr6:32088573 | GTAA | G | 341 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2779+209_2779+211d others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088573 | |||||||
chr6:32088729 | A | G | 1 | a0003c0003t0002g0345 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2779+56T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088729 | |||||||
chr6:32089113 | A | G | 1 | a0010c0087t0002g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2516-65T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089113 | |||||||
chr6:32089130 | C | G | 5 | a0006c0006t0001g0312 a0006c0006t0001g0314 a0006c0006t0001g0330 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2516-82G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089130 | |||||||
chr6:32089143 | TCTGCCCT others(7): Show |
T | 1 | a0096c0063t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2515+66_2515+79del others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089143 | |||||||
chr6:32089531 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2359-152C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089531 | |||||||
chr6:32089565 | G | A | 1 | a0015c0014t0001g0287 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2359-186C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089565 | |||||||
chr6:32089848 | C | T | 7 | a0022c0028t0002g0213 a0022c0028t0002g0214 a0022c0028t0002g0215 others(4): Show |
8 | HG01243.hp1 HG02738.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.2359-469G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089848 | |||||||
chr6:32089850 | C | T | 57 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(54): Show |
64 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2359-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089850 | |||||||
chr6:32090113 | C | T | 1 | a0067c0060t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2359-734G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090113 | |||||||
chr6:32090195 | T | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2359-816A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090195 | |||||||
chr6:32090357 | G | A | 1 | a0039c0038t0002g0096 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2359-978C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090357 | |||||||
chr6:32090454 | C | G | 1 | a0006c0045t0001g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2359-1075G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090454 | |||||||
chr6:32090484 | C | T | 1 | a0049c0055t0002g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2359-1105G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090484 | |||||||
chr6:32090648 | G | C | 20 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(17): Show |
25 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359-1269C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090648 | |||||||
chr6:32090899 | C | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0156 a0001c0001t0001g0159 others(13): Show |
16 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2359-1520G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090899 | |||||||
chr6:32091171 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2359-1792G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091171 | |||||||
chr6:32091173 | C | T | 1 | a0042c0070t0002g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2359-1794G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091173 | |||||||
chr6:32091203 | C | T | 1 | a0001c0109t0001g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2359-1824G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091203 | |||||||
chr6:32091204 | G | A | 1 | a0011c0009t0002g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2359-1825C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091204 | |||||||
chr6:32091298 | C | T | 3 | a0020c0026t0001g0167 a0020c0058t0001g0165 a0085c0059t0001g0163 |
3 | NA18941.hp1 NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2359-1919G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091298 | |||||||
chr6:32091480 | AT | A | 6 | a0002c0002t0001g0133 a0019c0022t0002g0333 a0019c0022t0002g0334 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2359-2102delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091480 | |||||||
chr6:32091511 | CTT | C | 3 | a0021c0027t0001g0008 a0021c0027t0001g0174 a0069c0065t0002g0175 |
5 | HG02129.hp2 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2359-2134_2359-213 others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091511 | |||||||
chr6:32091623 | C | T | 17 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(14): Show |
19 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2359-2244G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091623 | |||||||
chr6:32091674 | A | G | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.2359-2295T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091674 | |||||||
chr6:32091897 | C | G | 37 | a0003c0003t0001g0342 a0003c0003t0002g0053 a0003c0003t0002g0242 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2359-2518G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091897 | |||||||
chr6:32092090 | A | G | 5 | a0016c0025t0002g0052 a0016c0025t0002g0087 a0016c0025t0002g0088 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2359-2711T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092090 | |||||||
chr6:32092436 | G | C | 64 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(61): Show |
72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2358+2640C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092436 | |||||||
chr6:32092516 | C | T | 1 | a0009c0029t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2358+2560G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092516 | |||||||
chr6:32092690 | CA | C | 255 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2358+2385delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092690 | |||||||
chr6:32092690 | CAA | C | 20 | a0001c0001t0001g0267 a0002c0040t0002g0086 a0002c0040t0002g0094 others(17): Show |
21 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.2358+2384_2358+238 others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092690 | |||||||
chr6:32092715 | A | G | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2358+2361T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092715 | |||||||
chr6:32092719 | G | C | 14 | a0011c0009t0002g0002 a0011c0009t0002g0050 a0011c0009t0002g0057 others(11): Show |
17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2358+2357C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092719 | |||||||
chr6:32092780 | A | G | 12 | a0005c0013t0001g0228 a0005c0013t0001g0231 a0005c0013t0001g0232 others(9): Show |
12 | HG00438.hp1 HG02132.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.2358+2296T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092780 | |||||||
chr6:32092822 | G | A | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2358+2254C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092822 | |||||||
chr6:32093038 | T | C | 6 | a0005c0024t0001g0219 a0005c0024t0001g0220 a0005c0024t0001g0221 others(3): Show |
6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2358+2038A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093038 | |||||||
chr6:32093365 | T | A | 1 | a0055c0111t0001g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2358+1711A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093365 | |||||||
chr6:32093448 | G | A | 4 | a0025c0033t0002g0152 a0025c0033t0002g0153 a0025c0033t0002g0155 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2358+1628C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093448 | |||||||
chr6:32093562 | T | G | 18 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0113 others(15): Show |
22 | HG04204.hp1 NA18940.hp1 NA18950.hp2 others(19): Show |
intron_variant | MODIFIER | c.2358+1514A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093562 | |||||||
chr6:32093888 | A | G | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2358+1188T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093888 | |||||||
chr6:32093997 | G | A | 1 | a0096c0063t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+1079C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093997 | |||||||
chr6:32094095 | C | CA | 78 | a0001c0001t0001g0111 a0001c0001t0001g0267 a0001c0001t0001g0285 others(75): Show |
84 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2358+980dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | |||||||
chr6:32094095 | C | CAA | 35 | a0002c0042t0002g0142 a0004c0008t0001g0138 a0004c0008t0001g0187 others(32): Show |
37 | HG00438.hp1 HG01069.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2358+979_2358+980d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | |||||||
chr6:32094095 | CA | C | 118 | a0001c0001t0001g0107 a0001c0001t0001g0241 a0001c0001t0001g0255 others(115): Show |
125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.2358+980delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | |||||||
chr6:32094095 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0265 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2358+968_2358+980d others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | |||||||
chr6:32094475 | C | T | 19 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(16): Show |
19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2358+601G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094475 | |||||||
chr6:32094603 | T | G | 12 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(9): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.2358+473A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094603 | |||||||
chr6:32094691 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2358+385C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094691 | |||||||
chr6:32094910 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2358+166C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094910 | |||||||
chr6:32094981 | C | G | 1 | a0061c0076t0002g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2358+95G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094981 | |||||||
chr6:32095325 | CAG | C | 26 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(23): Show |
27 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2243-136_2243-135d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/43 | chr6 | 32095325 | |||||||
chr6:32095593 | G | C | 2 | a0009c0020t0001g0051 a0089c0090t0002g0143 |
2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2242+18C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/43 | chr6 | 32095593 | |||||||
chr6:32097483 | C | G | 1 | a0001c0034t0001g0254 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.404-34G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/43 | chr6 | 32097483 | |||||||
chr6:32098345 | G | A | 2 | a0010c0010t0002g0009 a0010c0010t0002g0033 |
3 | HG01099.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-139C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098345 | |||||||
chr6:32098366 | T | C | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-160A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098366 | |||||||
chr6:32098400 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
80 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-8-194A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098400 | |||||||
chr6:32098443 | C | T | 4 | a0010c0010t0002g0009 a0010c0010t0002g0029 a0010c0010t0002g0032 others(1): Show |
5 | HG01074.hp1 HG01099.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-237G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098443 | |||||||
chr6:32098456 | T | TTTTTG | 25 | a0002c0002t0001g0011 a0005c0013t0001g0045 a0005c0013t0001g0228 others(22): Show |
26 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-255_-8-251dupCA others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | |||||||
chr6:32098456 | TTTTTG | T | 8 | a0004c0011t0001g0178 a0004c0011t0001g0179 a0004c0011t0001g0190 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-255_-8-251delCA others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | |||||||
chr6:32098456 | TTTTTGTT others(3): Show |
T | 25 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(22): Show |
26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-260_-8-251delCA others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | |||||||
chr6:32098543 | C | T | 15 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(12): Show |
17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-337G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098543 | |||||||
chr6:32098670 | G | A | 37 | a0002c0040t0002g0086 a0002c0040t0002g0094 a0005c0013t0001g0045 others(34): Show |
38 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-464C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098670 | |||||||
chr6:32098858 | T | A | 1 | a0087c0124t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-652A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098858 | |||||||
chr6:32098936 | A | G | 1 | a0010c0010t0002g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-730T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098936 | |||||||
chr6:32098969 | T | C | 2 | a0035c0043t0002g0037 a0035c0043t0002g0137 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-763A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098969 | |||||||
chr6:32098988 | C | T | 25 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(22): Show |
26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-782G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098988 | |||||||
chr6:32099038 | C | T | 15 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(12): Show |
17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-832G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099038 | |||||||
chr6:32099042 | T | A | 341 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-8-836A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099042 | |||||||
chr6:32099226 | T | C | 16 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(13): Show |
18 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1020A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099226 | |||||||
chr6:32099235 | CT | C | 130 | a0001c0001t0001g0036 a0001c0001t0001g0285 a0002c0002t0001g0113 others(127): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-8-1030delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | |||||||
chr6:32099235 | CTT | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-8-1031_-8-1030del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | |||||||
chr6:32099235 | CTTT | C | 20 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(17): Show |
20 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1032_-8-1030del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | |||||||
chr6:32099658 | T | G | 17 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0011c0009t0002g0002 others(14): Show |
20 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-1452A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099658 | |||||||
chr6:32099659 | TG | T | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1454delC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099659 | |||||||
chr6:32099661 | G | C | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1455C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099661 | |||||||
chr6:32099726 | GA | G | 55 | a0001c0001t0001g0292 a0002c0040t0002g0086 a0002c0040t0002g0094 others(52): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-8-1521delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099726 | |||||||
chr6:32099946 | T | TA | 85 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0241 others(82): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-1741dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | |||||||
chr6:32099946 | T | TAA | 11 | a0012c0015t0001g0324 a0012c0015t0001g0327 a0012c0098t0001g0325 others(8): Show |
11 | HG01891.hp1 HG01975.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-1742_-8-1741dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | |||||||
chr6:32099946 | TA | T | 23 | a0004c0008t0001g0177 a0007c0004t0001g0197 a0008c0005t0002g0004 others(20): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-1741delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | |||||||
chr6:32099966 | AAAAAC | A | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1765_-8-1761del others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099966 | |||||||
chr6:32100065 | A | G | 1 | a0002c0002t0001g0011 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-8-1859T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100065 | |||||||
chr6:32100107 | CT | C | 40 | a0001c0001t0001g0299 a0001c0007t0001g0274 a0001c0007t0001g0282 others(37): Show |
41 | HG00140.hp1 HG01071.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-8-1902delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100107 | |||||||
chr6:32100173 | C | T | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1967G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100173 | |||||||
chr6:32100190 | C | T | 24 | a0001c0001t0001g0036 a0009c0020t0001g0051 a0009c0020t0001g0075 others(21): Show |
24 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-1984G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100190 | |||||||
chr6:32100328 | C | T | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2122G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100328 | |||||||
chr6:32100405 | G | C | 1 | a0035c0043t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-2199C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100405 | |||||||
chr6:32100653 | G | A | 1 | a0092c0121t0001g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-2447C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100653 | |||||||
chr6:32100714 | G | A | 1 | a0057c0122t0004g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-8-2508C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100714 | |||||||
chr6:32100718 | C | T | 2 | a0013c0018t0002g0010 a0013c0080t0002g0084 |
3 | HG00323.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-8-2512G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100718 | |||||||
chr6:32100845 | G | T | 1 | a0004c0061t0001g0176 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-2639C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100845 | |||||||
chr6:32101029 | G | C | 1 | a0049c0055t0002g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8-2823C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101029 | |||||||
chr6:32101077 | C | CA | 51 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0160 others(48): Show |
55 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-2872dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | C | CAA | 52 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0107 others(49): Show |
54 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-8-2873_-8-2872dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | C | CAAA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0109 a0001c0001t0001g0110 others(24): Show |
31 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-2874_-8-2872dup others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | C | CAAAA | 8 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0270 others(5): Show |
8 | HG01358.hp2 HG02055.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-2875_-8-2872dup others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | CA | C | 52 | a0002c0002t0001g0117 a0002c0012t0002g0043 a0003c0003t0002g0242 others(49): Show |
55 | HG00140.hp1 HG00408.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-2872delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | CAA | C | 25 | a0003c0003t0002g0249 a0003c0003t0002g0307 a0003c0003t0002g0345 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-2873_-8-2872del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101077 | CAAA | C | 11 | a0003c0003t0001g0342 a0003c0003t0002g0343 a0003c0003t0002g0344 others(8): Show |
11 | HG00408.hp2 HG00609.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-2874_-8-2872del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | |||||||
chr6:32101108 | G | A | 10 | a0004c0008t0001g0309 a0007c0004t0001g0001 a0007c0004t0001g0193 others(7): Show |
14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-2902C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101108 | |||||||
chr6:32101179 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-8-2973T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101179 | |||||||
chr6:32101455 | A | T | 1 | a0012c0015t0001g0327 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8-3249T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101455 | |||||||
chr6:32101491 | G | A | 1 | a0012c0015t0001g0327 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8-3285C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101491 | |||||||
chr6:32101512 | A | T | 2 | a0057c0122t0004g0226 a0073c0123t0004g0225 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-8-3306T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101512 | |||||||
chr6:32101588 | C | CT | 64 | a0001c0001t0001g0105 a0001c0001t0001g0145 a0001c0001t0001g0151 others(61): Show |
71 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-8-3383dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101588 | |||||||
chr6:32101588 | C | CTT | 62 | a0002c0002t0001g0116 a0002c0002t0001g0202 a0002c0012t0002g0042 others(59): Show |
70 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-3384_-8-3383dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101588 | |||||||
chr6:32101608 | T | C | 1 | a0001c0109t0001g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-3402A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101608 | |||||||
chr6:32101855 | C | G | 1 | a0002c0042t0002g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8-3649G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101855 | |||||||
chr6:32102029 | G | C | 369 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(366): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-8-3823C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102029 | |||||||
chr6:32102064 | C | T | 1 | a0052c0116t0001g0370 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-3858G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102064 | |||||||
chr6:32102236 | G | C | 1 | a0020c0026t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8-4030C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102236 | |||||||
chr6:32102292 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
78 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-8-4086C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102292 | |||||||
chr6:32102297 | G | A | 14 | a0001c0007t0001g0273 a0001c0007t0001g0274 a0001c0007t0001g0275 others(11): Show |
14 | HG00733.hp1 HG01346.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-4091C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102297 | |||||||
chr6:32102462 | A | G | 11 | a0008c0005t0002g0004 a0008c0005t0002g0047 a0008c0005t0002g0063 others(8): Show |
13 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-4256T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102462 | |||||||
chr6:32102498 | A | G | 1 | a0068c0097t0002g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-4292T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102498 | |||||||
chr6:32102570 | AAAAAAAG | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(140): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-8-4371_-8-4365del others(7): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102570 | |||||||
chr6:32102585 | A | T | 1 | a0025c0033t0002g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-8-4379T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102585 | |||||||
chr6:32102746 | CCT | C | 34 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(31): Show |
39 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8-4542_-8-4541del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102746 | |||||||
chr6:32102825 | CA | C | 5 | a0017c0017t0003g0205 a0017c0017t0003g0206 a0017c0017t0003g0207 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4620delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102825 | |||||||
chr6:32102913 | T | A | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4707A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102913 | |||||||
chr6:32102938 | A | C | 3 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 |
3 | HG00408.hp1 HG00597.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-8-4732T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102938 | |||||||
chr6:32103061 | T | C | 15 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(12): Show |
16 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-4855A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103061 | |||||||
chr6:32103108 | T | C | 1 | a0055c0111t0001g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8-4902A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103108 | |||||||
chr6:32103114 | T | G | 1 | a0058c0105t0001g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-8-4908A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103114 | |||||||
chr6:32103187 | A | T | 1 | a0010c0010t0002g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-4981T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103187 | |||||||
chr6:32103231 | G | A | 15 | a0001c0007t0001g0272 a0001c0007t0001g0273 a0001c0007t0001g0274 others(12): Show |
15 | HG00639.hp1 HG00733.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-5025C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103231 | |||||||
chr6:32103233 | G | A | 27 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0243 others(24): Show |
27 | HG00140.hp1 HG01109.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-5027C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103233 | |||||||
chr6:32103240 | C | G | 341 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-8-5034G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103240 | |||||||
chr6:32103250 | G | A | 1 | a0002c0095t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-5044C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103250 | |||||||
chr6:32103271 | T | TA | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-5066dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103271 | |||||||
chr6:32103335 | C | T | 3 | a0001c0001t0001g0247 a0033c0049t0002g0245 a0033c0049t0002g0246 |
3 | HG00639.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-8-5129G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103335 | |||||||
chr6:32103422 | TC | T | 17 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0011c0009t0002g0002 others(14): Show |
20 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-5217delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103422 | |||||||
chr6:32103429 | C | CA | 207 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(204): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-8-5224dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103429 | |||||||
chr6:32103429 | CA | C | 8 | a0002c0002t0001g0113 a0003c0003t0002g0053 a0009c0029t0001g0055 others(5): Show |
8 | HG02486.hp1 HG02965.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-5224delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103429 | |||||||
chr6:32103478 | C | A | 1 | a0002c0096t0002g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-8-5272G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103478 | |||||||
chr6:32103481 | C | G | 10 | a0012c0015t0001g0320 a0012c0015t0001g0321 a0012c0015t0001g0323 others(7): Show |
11 | HG02622.hp1 HG02735.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-5275G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103481 | |||||||
chr6:32103491 | CCA | C | 13 | a0006c0006t0001g0218 a0006c0006t0001g0311 a0006c0006t0001g0312 others(10): Show |
13 | HG00140.hp1 HG01884.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-5287_-8-5286del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103491 | |||||||
chr6:32103607 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-5401G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103607 | |||||||
chr6:32103662 | A | T | 1 | a0001c0109t0001g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-5456T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103662 | |||||||
chr6:32103727 | C | CT | 43 | a0001c0001t0001g0243 a0002c0012t0002g0041 a0003c0003t0002g0242 others(40): Show |
44 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-9+5453dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | |||||||
chr6:32103727 | C | CTT | 6 | a0006c0006t0001g0311 a0019c0022t0002g0333 a0019c0022t0002g0334 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+5452_-9+5453dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | |||||||
chr6:32103727 | CT | C | 15 | a0001c0001t0001g0299 a0002c0002t0001g0135 a0004c0011t0001g0198 others(12): Show |
17 | HG01074.hp2 HG01934.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+5453delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | |||||||
chr6:32103806 | A | C | 1 | a0009c0091t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9+5375T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103806 | |||||||
chr6:32103812 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-9+5369G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103812 | |||||||
chr6:32103860 | T | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(141): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-9+5321A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103860 | |||||||
chr6:32103889 | A | G | 21 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(18): Show |
21 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9+5292T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103889 | |||||||
chr6:32104116 | C | T | 341 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-9+5065G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104116 | |||||||
chr6:32104208 | C | T | 1 | a0008c0005t0002g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-9+4973G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104208 | |||||||
chr6:32104434 | A | C | 15 | a0020c0026t0001g0164 a0020c0026t0001g0167 a0020c0026t0001g0172 others(12): Show |
15 | HG02129.hp1 HG02698.hp1 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+4747T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104434 | |||||||
chr6:32104596 | C | T | 1 | a0010c0087t0002g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9+4585G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104596 | |||||||
chr6:32104618 | A | G | 18 | a0005c0013t0001g0045 a0005c0013t0001g0228 a0005c0013t0001g0231 others(15): Show |
18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+4563T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104618 | |||||||
chr6:32104643 | C | T | 1 | a0005c0013t0001g0228 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9+4538G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104643 | |||||||
chr6:32105152 | T | A | 1 | a0044c0089t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-9+4029A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105152 | |||||||
chr6:32105163 | C | T | 63 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(60): Show |
71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.-9+4018G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105163 | |||||||
chr6:32105463 | GAGGGC | G | 4 | a0002c0012t0002g0041 a0002c0012t0002g0042 a0002c0012t0002g0043 others(1): Show |
4 | HG00408.hp1 HG00597.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+3713_-9+3717del others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105463 | |||||||
chr6:32105581 | C | T | 1 | a0051c0104t0001g0300 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-9+3600G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105581 | |||||||
chr6:32105639 | C | T | 1 | a0037c0041t0001g0040 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9+3542G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105639 | |||||||
chr6:32105762 | A | T | 1 | a0010c0010t0002g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+3419T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105762 | |||||||
chr6:32105800 | A | C | 1 | a0005c0013t0001g0228 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9+3381T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105800 | |||||||
chr6:32105923 | C | T | 56 | a0004c0008t0001g0014 a0004c0008t0001g0038 a0004c0008t0001g0138 others(53): Show |
58 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+3258G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105923 | |||||||
chr6:32105929 | A | G | 2 | a0035c0043t0002g0037 a0035c0043t0002g0137 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+3252T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105929 | |||||||
chr6:32106122 | G | C | 1 | a0062c0117t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9+3059C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106122 | |||||||
chr6:32106131 | T | TG | 47 | a0001c0001t0001g0036 a0001c0001t0001g0145 a0001c0001t0001g0159 others(44): Show |
48 | HG00408.hp2 HG00609.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9+3049dupC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106131 | |||||||
chr6:32106134 | G | C | 7 | a0008c0005t0002g0147 a0022c0028t0002g0213 a0022c0028t0002g0214 others(4): Show |
8 | HG01884.hp1 HG02738.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3047C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106134 | |||||||
chr6:32106136 | G | C | 10 | a0010c0010t0002g0009 a0010c0010t0002g0029 a0010c0010t0002g0032 others(7): Show |
11 | HG00642.hp1 HG01074.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+3045C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106136 | |||||||
chr6:32106140 | G | C | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-9+3041C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106140 | |||||||
chr6:32106196 | T | C | 15 | a0001c0001t0001g0151 a0003c0003t0002g0307 a0014c0016t0002g0347 others(12): Show |
15 | HG00408.hp2 HG00609.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+2985A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106196 | |||||||
chr6:32106247 | A | G | 14 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0003c0003t0001g0342 others(11): Show |
14 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+2934T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106247 | |||||||
chr6:32106256 | G | A | 3 | a0006c0006t0001g0330 a0006c0006t0001g0331 a0006c0006t0001g0332 |
3 | HG01884.hp2 HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-9+2925C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106256 | |||||||
chr6:32106301 | G | A | 1 | a0020c0026t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+2880C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106301 | |||||||
chr6:32106514 | C | T | 1 | a0004c0011t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+2667G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106514 | |||||||
chr6:32106657 | C | T | 1 | a0020c0026t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+2524G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106657 | |||||||
chr6:32106672 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9+2509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106672 | |||||||
chr6:32106734 | C | T | 1 | a0065c0085t0002g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-9+2447G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106734 | |||||||
chr6:32106741 | C | G | 13 | a0010c0010t0001g0022 a0010c0010t0002g0009 a0010c0010t0002g0024 others(10): Show |
14 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+2440G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106741 | |||||||
chr6:32106772 | T | C | 1 | a0014c0016t0006g0368 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-9+2409A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106772 | |||||||
chr6:32107027 | T | C | 30 | a0004c0008t0001g0309 a0006c0006t0001g0218 a0006c0006t0001g0311 others(27): Show |
35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9+2154A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107027 | |||||||
chr6:32107078 | C | T | 1 | a0045c0088t0001g0023 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-9+2103G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107078 | |||||||
chr6:32107114 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9+2067A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107114 | |||||||
chr6:32107137 | C | T | 1 | a0010c0010t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+2044G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107137 | |||||||
chr6:32107157 | C | T | 1 | a0027c0035t0001g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+2024G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107157 | |||||||
chr6:32107220 | C | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0020c0026t0001g0157 others(3): Show |
7 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+1961G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107220 | |||||||
chr6:32107526 | T | C | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+1655A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107526 | |||||||
chr6:32107582 | T | C | 5 | a0019c0022t0002g0333 a0019c0022t0002g0334 a0019c0022t0002g0335 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+1599A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107582 | |||||||
chr6:32107766 | A | C | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1415T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107766 | |||||||
chr6:32107767 | C | A | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1414G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107767 | |||||||
chr6:32107768 | A | C | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1413T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107768 | |||||||
chr6:32107770 | ATGGGGGT others(8): Show |
A | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1396_-9+1410del others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107770 | |||||||
chr6:32107786 | T | C | 199 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0224 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-9+1395A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107786 | |||||||
chr6:32107787 | G | A | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1394C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107787 | |||||||
chr6:32107789 | C | G | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1392G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107789 | |||||||
chr6:32107790 | C | A | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1391G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107790 | |||||||
chr6:32107792 | C | G | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1389G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107792 | |||||||
chr6:32107799 | C | T | 1 | a0053c0118t0002g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1382G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107799 | |||||||
chr6:32107963 | A | G | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+1218T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107963 | |||||||
chr6:32107988 | G | A | 2 | a0024c0052t0002g0018 a0024c0125t0002g0369 |
3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+1193C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107988 | |||||||
chr6:32108023 | A | G | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+1158T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108023 | |||||||
chr6:32108059 | G | A | 6 | a0001c0001t0001g0224 a0005c0024t0001g0219 a0005c0024t0001g0220 others(3): Show |
6 | HG01952.hp1 HG02165.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1122C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108059 | |||||||
chr6:32108335 | G | A | 1 | a0076c0064t0001g0338 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+846C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108335 | |||||||
chr6:32108361 | C | G | 2 | a0008c0005t0002g0340 a0053c0118t0002g0020 |
2 | HG01934.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-9+820G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108361 | |||||||
chr6:32108561 | G | A | 1 | a0007c0004t0001g0339 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9+620C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108561 | |||||||
chr6:32108578 | T | C | 3 | a0057c0122t0004g0226 a0073c0123t0004g0225 a0093c0119t0004g0227 |
3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+603A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108578 | |||||||
chr6:32108640 | C | T | 1 | a0079c0081t0002g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+541G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108640 | |||||||
chr6:32108722 | G | A | 115 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0240 others(112): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-9+459C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108722 | |||||||
chr6:32109065 | C | A | 31 | a0003c0003t0001g0342 a0003c0003t0002g0343 a0003c0003t0002g0344 others(28): Show |
32 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-9+116G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32109065 | |||||||
chr6:32109130 | G | A | 3 | a0052c0116t0001g0370 a0059c0078t0001g0371 a0070c0079t0001g0372 |
3 | HG01891.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+51C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32109130 |