geneid | 221336 |
---|---|
ensemblid | ENSG00000151917.18 |
hgncid | 20871 |
symbol | BEND6 |
name | BEN domain containing 6 |
refseq_nuc | NM_152731.3 |
refseq_prot | NP_689944.2 |
ensembl_nuc | ENST00000370746.8 |
ensembl_prot | ENSP00000359782.3 |
mane_status | MANE Select |
chr | chr6 |
start | 56955107 |
end | 57027346 |
strand | + |
ver | v1.2 |
region | chr6:56955107-57027346 |
region5000 | chr6:56950107-57032346 |
regionname0 | BEND6_chr6_56955107_57027346 |
regionname5000 | BEND6_chr6_56950107_57032346 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 279 | 204 | 66 | 38 | 80 | 4 | 14 | 52 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1729 | 112 | 31 | 23 | 45 | 3 | 9 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0002 | 1/0 | 1729 | 59 | 28 | 8 | 21 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0003 | 0/0 | 1729 | 13 | 4 | 5 | 0 | 1 | 3 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0004 | 0/0 | 1729 | 11 | 1 | 0 | 10 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0005 | 0/0 | 1729 | 4 | 0 | 0 | 4 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0006 | 0/0 | 1729 | 2 | 0 | 1 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0007 | 0/0 | 1729 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0008 | 0/0 | 1729 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
t0009 | 0/0 | 1729 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0002 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 840 | 203 | 65 | 38 | 80 | 4 | 14 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0002 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2568 | 112 | 31 | 23 | 45 | 3 | 9 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0002 | 1/0 | 2568 | 58 | 27 | 8 | 21 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0003 | 0/0 | 2568 | 13 | 4 | 5 | 0 | 1 | 3 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0004 | 0/0 | 2568 | 11 | 1 | 0 | 10 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0005 | 0/0 | 2568 | 4 | 0 | 0 | 4 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0006 | 0/0 | 2568 | 2 | 0 | 1 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0007 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0008 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0001t0009 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
a0001c0002t0002 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | copy fasta | chr6 | 56950107 | 57032346 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0002 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0092 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | IBS | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CDX | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0178 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0179 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | YRI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | YRI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | USA | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | USA | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0143 | AFR | LWK | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0130 | REF | REF | BEND6_chr6_56950107_57032346 | BEND6 | chr6 | 56950107 | 57032346 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56992503
|
A | G | 1 | a0001c0002 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.246A>G | p.Thr82Thr | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/7 | 700/2568 | 246/840 | 82/279 | chr6 | 56992503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56955157
|
G | A | 1 | a0001c0001t0007 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-404G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/7 | 26654 | chr6 | 56955157 | |||||
chr6:56955365
|
G | A | 2 | a0001c0001t0001a0001c0001t0008 | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/7 | 26446 | chr6 | 56955365 | |||||
chr6:56955450
|
A | G | 3 | a0001c0001t0003a0001c0001t0006a0001c0001t0009 | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-111A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/7 | 26361 | chr6 | 56955450 | |||||
chr6:57026330
|
A | G | 1 | a0001c0001t0004 | 11 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*258A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 7/7 | 7782 | chr6 | 57026330 | |||||
chr6:57026615
|
C | G | 1 | a0001c0001t0009 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*543C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 7/7 | 8067 | chr6 | 57026615 | |||||
chr6:57027181
|
G | A | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0008 | 18 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1109G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 7/7 | 8633 | chr6 | 57027181 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56955561
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0004g0180 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-101+101C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56955561 | ||||||
chr6:56955607
|
C | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+147C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56955607 | ||||||
chr6:56955742
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-101+282G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56955742 | ||||||
chr6:56955879
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-101+419C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56955879 | ||||||
chr6:56956027
|
A | G | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+567A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56956027 | ||||||
chr6:56956393
|
G | T | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-101+933G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56956393 | ||||||
chr6:56956563
|
T | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101+1103T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56956563 | ||||||
chr6:56956569
|
T | C | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-101+1109T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56956569 | ||||||
chr6:56957114
|
A | C | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+1654A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56957114 | ||||||
chr6:56957507
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-101+2047A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56957507 | ||||||
chr6:56957601
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-101+2141T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56957601 | ||||||
chr6:56957820
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-101+2360G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56957820 | ||||||
chr6:56957833
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-101+2373G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56957833 | ||||||
chr6:56958089
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-101+2629C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958089 | ||||||
chr6:56958109
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-101+2649A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958109 | ||||||
chr6:56958200
|
C | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101+2740C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958200 | ||||||
chr6:56958217
|
G | C | 53 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(50): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-101+2757G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958217 | ||||||
chr6:56958303
|
G | C | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101+2843G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958303 | ||||||
chr6:56958570
|
C | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101+3110C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958570 | ||||||
chr6:56958627
|
T | C | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101+3167T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56958627 | ||||||
chr6:56959251
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-101+3791C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56959251 | ||||||
chr6:56959493
|
A | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101+4033A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56959493 | ||||||
chr6:56959773
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-101+4313T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56959773 | ||||||
chr6:56959849
|
C | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-101+4389C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56959849 | ||||||
chr6:56960027
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG01433.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101+4567C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960027 | ||||||
chr6:56960282
|
AT | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-101+4823delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960282 | ||||||
chr6:56960316
|
G | T | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-101+4856G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960316 | ||||||
chr6:56960452
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-101+4992G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960452 | ||||||
chr6:56960828
|
G | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-101+5368G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960828 | ||||||
chr6:56960942
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-101+5482A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56960942 | ||||||
chr6:56960992
|
TGTAGAA | T | 29 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(26): Show | 36 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.-101+5535_-101+554 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56960992 | |||||
chr6:56961026
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-101+5566T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961026 | ||||||
chr6:56961057
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-101+5597G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961057 | ||||||
chr6:56961460
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-101+6000C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961460 | ||||||
chr6:56961532
|
T | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 41 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-101+6072T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961532 | ||||||
chr6:56961680
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+6220G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961680 | ||||||
chr6:56961739
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-101+6279C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961739 | ||||||
chr6:56961758
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-101+6298C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961758 | ||||||
chr6:56961915
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+6455G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56961915 | ||||||
chr6:56962009
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-101+6549G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56962009 | ||||||
chr6:56962175
|
A | T | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-101+6715A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56962175 | ||||||
chr6:56962689
|
T | C | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.-101+7229T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56962689 | ||||||
chr6:56962830
|
G | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 190 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.-101+7370G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56962830 | ||||||
chr6:56962947
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01952.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-101+7487T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56962947 | ||||||
chr6:56963138
|
T | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101+7678T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56963138 | ||||||
chr6:56963334
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-101+7874C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56963334 | ||||||
chr6:56963433
|
A | G | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02976.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-101+7973A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56963433 | ||||||
chr6:56963832
|
TATA | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+8376_-101+837 others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56963832 | |||||
chr6:56963953
|
G | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+8493G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56963953 | ||||||
chr6:56964006
|
ATAG | A | 40 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(37): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-101+8552_-101+855 others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56964006 | |||||
chr6:56964058
|
T | A | 1 | a0001c0001t0007g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-101+8598T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56964058 | ||||||
chr6:56964142
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-101+8682A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56964142 | ||||||
chr6:56964585
|
T | TC | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-101+9127dupC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56964585 | |||||
chr6:56964829
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-101+9369G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56964829 | ||||||
chr6:56964935
|
C | T | 1 | a0001c0001t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-101+9475C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56964935 | ||||||
chr6:56965132
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 104 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-101+9672C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965132 | ||||||
chr6:56965164
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02145.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-101+9704A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965164 | ||||||
chr6:56965196
|
A | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+9736A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965196 | ||||||
chr6:56965239
|
T | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+9779T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965239 | ||||||
chr6:56965325
|
G | GCA | 2 | a0001c0001t0003g0170a0001c0001t0006g0171 | 2 | HG00733.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-101+9868_-101+986 others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965325 | |||||
chr6:56965440
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01884.hp1 HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-101+9980G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965440 | ||||||
chr6:56965466
|
C | T | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-101+10006C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965466 | ||||||
chr6:56965669
|
A | C | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-101+10209A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965669 | ||||||
chr6:56965676
|
T | TTA | 26 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0029others(23): Show | 28 | HG00558.hp1 HG01358.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.-101+10242_-101+10 others(8): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
T | TTATA | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG02683.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-101+10240_-101+10 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
T | TTATATA | 2 | a0001c0001t0001g0134a0001c0001t0002g0125 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-101+10238_-101+10 others(12): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0028 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-101+10234_-101+10 others(16): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
TTA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0064others(7): Show | 12 | HG00741.hp2 HG01952.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-101+10242_-101+10 others(8): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
TTATA | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+10240_-101+10 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
TTATATA | T | 3 | a0001c0001t0001g0138a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01884.hp2 HG03195.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-101+10238_-101+10 others(12): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965676
|
TTATATAT others(1): Show |
T | 37 | a0001c0001t0001g0124a0001c0001t0002g0001a0001c0001t0002g0003others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-101+10236_-101+10 others(14): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56965676 | |||||
chr6:56965751
|
G | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+10291G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965751 | ||||||
chr6:56965885
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 6 | HG02027.hp1 NA18939.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-101+10425A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56965885 | ||||||
chr6:56966097
|
G | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+10637G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966097 | ||||||
chr6:56966146
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-101+10686G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966146 | ||||||
chr6:56966353
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-101+10893C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966353 | ||||||
chr6:56966593
|
CAATT | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-101+11134_-101+11 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966593 | ||||||
chr6:56966666
|
T | C | 10 | a0001c0001t0002g0003a0001c0001t0002g0145a0001c0001t0002g0146others(7): Show | 12 | HG00741.hp1 HG01099.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-101+11206T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966666 | ||||||
chr6:56966696
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-101+11236G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966696 | ||||||
chr6:56966734
|
T | C | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101+11274T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966734 | ||||||
chr6:56966849
|
C | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+11389C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56966849 | ||||||
chr6:56967423
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-101+11963G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56967423 | ||||||
chr6:56967453
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-101+11993G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56967453 | ||||||
chr6:56967875
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-101+12415C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56967875 | ||||||
chr6:56967910
|
T | C | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101+12450T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56967910 | ||||||
chr6:56968031
|
T | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-101+12571T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968031 | ||||||
chr6:56968100
|
T | C | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-101+12640T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968100 | ||||||
chr6:56968312
|
C | CT | 31 | a0001c0001t0001g0013a0001c0001t0001g0118a0001c0001t0002g0001others(28): Show | 39 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-101+12878dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56968312 | |||||
chr6:56968312
|
C | CTT | 6 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG02027.hp2 HG02055.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+12877_-101+12 others(8): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56968312 | |||||
chr6:56968312
|
CT | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 104 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.-101+12878delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56968312 | |||||
chr6:56968312
|
CTT | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0078others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-101+12877_-101+12 others(8): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56968312 | |||||
chr6:56968312
|
CTTT | C | 10 | a0001c0001t0001g0079a0001c0001t0003g0002a0001c0001t0003g0169others(7): Show | 14 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101+12876_-101+12 others(9): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56968312 | |||||
chr6:56968365
|
G | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-101+12905G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968365 | ||||||
chr6:56968403
|
C | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-101+12943C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968403 | ||||||
chr6:56968460
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-101+13000G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968460 | ||||||
chr6:56968614
|
G | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-13097G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968614 | ||||||
chr6:56968650
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-100-13061C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968650 | ||||||
chr6:56968685
|
G | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-100-13026G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968685 | ||||||
chr6:56968832
|
T | C | 4 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0093others(1): Show | 4 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-12879T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968832 | ||||||
chr6:56968834
|
A | G | 53 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(50): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-100-12877A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968834 | ||||||
chr6:56968911
|
T | C | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-12800T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968911 | ||||||
chr6:56968918
|
A | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-100-12793A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968918 | ||||||
chr6:56968936
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-100-12775G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968936 | ||||||
chr6:56968952
|
G | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-12759G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56968952 | ||||||
chr6:56969030
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02145.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-100-12681C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969030 | ||||||
chr6:56969072
|
T | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-100-12639T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969072 | ||||||
chr6:56969073
|
CA | C | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-100-12627delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56969073 | |||||
chr6:56969387
|
G | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-100-12324G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969387 | ||||||
chr6:56969420
|
A | G | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-100-12291A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969420 | ||||||
chr6:56969554
|
A | C | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-12157A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969554 | ||||||
chr6:56969634
|
A | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-100-12077A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969634 | ||||||
chr6:56969697
|
T | G | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-12014T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969697 | ||||||
chr6:56969886
|
G | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-11825G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969886 | ||||||
chr6:56969910
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-100-11801G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56969910 | ||||||
chr6:56970270
|
C | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-100-11441C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970270 | ||||||
chr6:56970469
|
A | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-100-11242A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970469 | ||||||
chr6:56970557
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-100-11154C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970557 | ||||||
chr6:56970558
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0114others(1): Show | 4 | HG00673.hp1 HG01952.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-11153G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970558 | ||||||
chr6:56970743
|
A | G | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-10968A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970743 | ||||||
chr6:56970974
|
C | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-100-10737C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56970974 | ||||||
chr6:56971176
|
G | A | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-10535G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971176 | ||||||
chr6:56971311
|
C | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-10400C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971311 | ||||||
chr6:56971347
|
C | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-100-10364C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971347 | ||||||
chr6:56971511
|
G | T | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-10200G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971511 | ||||||
chr6:56971545
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-100-10166G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971545 | ||||||
chr6:56971596
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-100-10115A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971596 | ||||||
chr6:56971752
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-9959C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56971752 | ||||||
chr6:56972013
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-100-9698C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972013 | ||||||
chr6:56972085
|
T | TA | 2 | a0001c0001t0001g0094a0001c0001t0001g0137 | 2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-100-9626_-100-962 others(5): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972085 | ||||||
chr6:56972086
|
CT | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 106 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-100-9599delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56972086 | |||||
chr6:56972086
|
CTT | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.-100-9600_-100-959 others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56972086 | |||||
chr6:56972087
|
T | TGTC | 2 | a0001c0001t0001g0094a0001c0001t0001g0137 | 2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-100-9624_-100-962 others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972087 | ||||||
chr6:56972172
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-9539G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972172 | ||||||
chr6:56972447
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-9264G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972447 | ||||||
chr6:56972638
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0004g0063 | 2 | NA18943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-100-9073A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56972638 | ||||||
chr6:56973115
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-100-8596T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973115 | ||||||
chr6:56973261
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-100-8450C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973261 | ||||||
chr6:56973371
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-100-8340C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973371 | ||||||
chr6:56973500
|
TAATAAC | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-8204_-100-819 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56973500 | |||||
chr6:56973598
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-8113G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973598 | ||||||
chr6:56973686
|
A | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-8025A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973686 | ||||||
chr6:56973758
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-100-7953T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973758 | ||||||
chr6:56973784
|
T | A | 1 | a0001c0001t0001g0046 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-100-7927T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973784 | ||||||
chr6:56973909
|
G | A | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-7802G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973909 | ||||||
chr6:56973984
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-100-7727C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56973984 | ||||||
chr6:56974078
|
G | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-7633G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56974078 | ||||||
chr6:56974618
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-100-7093G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56974618 | ||||||
chr6:56974624
|
C | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-100-7087C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56974624 | ||||||
chr6:56974709
|
T | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-100-7002T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56974709 | ||||||
chr6:56974932
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-100-6779C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56974932 | ||||||
chr6:56975286
|
A | ATCACT | 56 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(53): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-100-6422_-100-642 others(9): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56975286 | |||||
chr6:56975363
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-100-6348A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975363 | ||||||
chr6:56975366
|
A | T | 1 | a0001c0001t0006g0171 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-100-6345A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975366 | ||||||
chr6:56975381
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | HG01884.hp2 HG03195.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-6330A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975381 | ||||||
chr6:56975523
|
A | G | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-6188A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975523 | ||||||
chr6:56975548
|
A | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-100-6163A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975548 | ||||||
chr6:56975601
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0043 | 3 | HG00639.hp2 HG00733.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-100-6110A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975601 | ||||||
chr6:56975755
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-5956C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975755 | ||||||
chr6:56975756
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01952.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-100-5955G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975756 | ||||||
chr6:56975780
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-100-5931A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975780 | ||||||
chr6:56975782
|
C | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-5929C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975782 | ||||||
chr6:56975877
|
A | AAC | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02145.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-100-5831_-100-583 others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56975877 | |||||
chr6:56975925
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-5786G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56975925 | ||||||
chr6:56976197
|
C | CT | 40 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(37): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-100-5498dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56976197 | |||||
chr6:56976218
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0098 | 3 | NA19065.hp1 NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-100-5493T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976218 | ||||||
chr6:56976272
|
T | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-100-5439T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976272 | ||||||
chr6:56976288
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18939.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-100-5423C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976288 | ||||||
chr6:56976296
|
C | T | 5 | a0001c0001t0001g0112a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-5415C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976296 | ||||||
chr6:56976297
|
G | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-5414G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976297 | ||||||
chr6:56976321
|
G | A | 1 | a0001c0001t0006g0171 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-100-5390G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976321 | ||||||
chr6:56976340
|
C | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100-5371C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976340 | ||||||
chr6:56976367
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG00558.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.-100-5344T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976367 | ||||||
chr6:56976474
|
C | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-5237C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976474 | ||||||
chr6:56976497
|
G | A | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-100-5214G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976497 | ||||||
chr6:56976601
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-100-5110G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976601 | ||||||
chr6:56976638
|
C | A | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-5073C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976638 | ||||||
chr6:56976668
|
G | A | 7 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(4): Show | 7 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-5043G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976668 | ||||||
chr6:56976749
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-4962C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976749 | ||||||
chr6:56976805
|
T | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-4906T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56976805 | ||||||
chr6:56977027
|
A | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-4684A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977027 | ||||||
chr6:56977126
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-4585G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977126 | ||||||
chr6:56977127
|
T | A | 1 | a0001c0001t0002g0153 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-100-4584T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977127 | ||||||
chr6:56977252
|
A | G | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-100-4459A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977252 | ||||||
chr6:56977254
|
G | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-4457G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977254 | ||||||
chr6:56977472
|
A | C | 2 | a0001c0001t0004g0061a0001c0002t0002g0133 | 2 | HG06807.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-100-4239A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977472 | ||||||
chr6:56977476
|
A | G | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-100-4235A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977476 | ||||||
chr6:56977477
|
T | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-4234T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977477 | ||||||
chr6:56977507
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-100-4204G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977507 | ||||||
chr6:56977822
|
T | C | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-3889T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977822 | ||||||
chr6:56977829
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-100-3882C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977829 | ||||||
chr6:56977862
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-100-3849C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977862 | ||||||
chr6:56977869
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0137 | 2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-100-3842A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977869 | ||||||
chr6:56977965
|
G | C | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-3746G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977965 | ||||||
chr6:56977992
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18939.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-100-3719T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56977992 | ||||||
chr6:56978068
|
C | G | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02976.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-100-3643C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978068 | ||||||
chr6:56978114
|
C | CA | 12 | a0001c0001t0001g0095a0001c0001t0003g0002a0001c0001t0003g0169others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-3585dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56978114 | |||||
chr6:56978241
|
C | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-3470C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978241 | ||||||
chr6:56978266
|
G | C | 1 | a0001c0001t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-100-3445G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978266 | ||||||
chr6:56978280
|
C | CTAAAA | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-100-3408_-100-340 others(9): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56978280 | |||||
chr6:56978496
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0116others(1): Show | 4 | HG00408.hp1 HG01496.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-3215C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978496 | ||||||
chr6:56978541
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-100-3170A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978541 | ||||||
chr6:56978728
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-100-2983G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978728 | ||||||
chr6:56978781
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-100-2930A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978781 | ||||||
chr6:56978917
|
C | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-2794C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56978917 | ||||||
chr6:56979154
|
A | G | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-2557A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56979154 | ||||||
chr6:56979741
|
A | G | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-100-1970A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56979741 | ||||||
chr6:56979837
|
A | G | 1 | a0001c0001t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-100-1874A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56979837 | ||||||
chr6:56979865
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-1846G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56979865 | ||||||
chr6:56979955
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-100-1756A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56979955 | ||||||
chr6:56980273
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-100-1438C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980273 | ||||||
chr6:56980333
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-100-1378C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980333 | ||||||
chr6:56980657
|
A | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 200 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.-100-1054A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980657 | ||||||
chr6:56980669
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-1042A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980669 | ||||||
chr6:56980836
|
T | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 104 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-100-875T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980836 | ||||||
chr6:56980916
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-100-795A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56980916 | ||||||
chr6:56981034
|
G | C | 7 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(4): Show | 7 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-677G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981034 | ||||||
chr6:56981133
|
A | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02976.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-100-578A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981133 | ||||||
chr6:56981172
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-100-539C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981172 | ||||||
chr6:56981307
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-100-404T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981307 | ||||||
chr6:56981317
|
C | T | 56 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(53): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-100-394C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981317 | ||||||
chr6:56981343
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-100-368G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981343 | ||||||
chr6:56981400
|
G | A | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-311G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981400 | ||||||
chr6:56981417
|
G | A | 7 | a0001c0001t0002g0003a0001c0001t0002g0146a0001c0001t0002g0147others(4): Show | 9 | HG00741.hp1 HG01099.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-100-294G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981417 | ||||||
chr6:56981536
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 180 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-100-175A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981536 | ||||||
chr6:56981586
|
AAATT | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02145.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-100-121_-100-118d others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 56981586 | |||||
chr6:56981665
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-100-46C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 1/6 | chr6 | 56981665 | ||||||
chr6:56982004
|
A | T | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.120+74A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982004 | ||||||
chr6:56982165
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.120+235C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982165 | ||||||
chr6:56982388
|
G | A | 29 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(26): Show | 36 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.120+458G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982388 | ||||||
chr6:56982395
|
A | G | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+465A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982395 | ||||||
chr6:56982579
|
G | T | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+649G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982579 | ||||||
chr6:56982634
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.120+704A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56982634 | ||||||
chr6:56983015
|
A | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.120+1085A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983015 | ||||||
chr6:56983198
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.120+1268A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983198 | ||||||
chr6:56983238
|
G | A | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+1308G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983238 | ||||||
chr6:56983254
|
C | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+1324C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983254 | ||||||
chr6:56983380
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.120+1450G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983380 | ||||||
chr6:56983653
|
G | T | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.120+1723G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983653 | ||||||
chr6:56983660
|
A | C | 1 | a0001c0001t0003g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.120+1730A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983660 | ||||||
chr6:56983820
|
C | T | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+1890C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983820 | ||||||
chr6:56983889
|
A | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+1959A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983889 | ||||||
chr6:56983941
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 202 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.120+2011A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56983941 | ||||||
chr6:56984044
|
C | T | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+2114C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56984044 | ||||||
chr6:56984249
|
GA | G | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+2328delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56984249 | |||||
chr6:56984412
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+2482G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56984412 | ||||||
chr6:56984717
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG01074.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.120+2787G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56984717 | ||||||
chr6:56984862
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.120+2932G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56984862 | ||||||
chr6:56985118
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.120+3188G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985118 | ||||||
chr6:56985150
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.120+3220C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985150 | ||||||
chr6:56985523
|
C | G | 47 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(44): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.120+3593C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985523 | ||||||
chr6:56985533
|
C | A | 47 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(44): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.120+3603C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985533 | ||||||
chr6:56985680
|
C | A | 6 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+3750C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985680 | ||||||
chr6:56985928
|
C | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+3998C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985928 | ||||||
chr6:56985961
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.120+4031C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56985961 | ||||||
chr6:56986071
|
C | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+4141C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986071 | ||||||
chr6:56986204
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0045 | 4 | HG01071.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+4274A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986204 | ||||||
chr6:56986286
|
G | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0068others(9): Show | 12 | HG01358.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+4356G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986286 | ||||||
chr6:56986309
|
G | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+4379G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986309 | ||||||
chr6:56986548
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+4618G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986548 | ||||||
chr6:56986959
|
T | C | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.120+5029T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56986959 | ||||||
chr6:56986973
|
CT | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0088others(29): Show | 37 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.120+5063delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56986973 | |||||
chr6:56986973
|
CTTT | C | 38 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(35): Show | 45 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.120+5061_120+5063d others(5): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56986973 | |||||
chr6:56987029
|
G | A | 1 | a0001c0001t0004g0057 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.120+5099G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987029 | ||||||
chr6:56987136
|
C | T | 1 | a0001c0001t0005g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.120+5206C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987136 | ||||||
chr6:56987154
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0166 | 2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.120+5224A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987154 | ||||||
chr6:56987159
|
T | C | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.121-5219T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987159 | ||||||
chr6:56987243
|
G | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 42 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.121-5135G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987243 | ||||||
chr6:56987251
|
A | T | 1 | a0001c0001t0002g0153 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.121-5127A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987251 | ||||||
chr6:56987361
|
T | C | 3 | a0001c0001t0002g0068a0001c0001t0002g0128a0001c0001t0002g0129 | 3 | HG03139.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-5017T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987361 | ||||||
chr6:56987437
|
G | A | 52 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(49): Show | 63 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.121-4941G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987437 | ||||||
chr6:56987444
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0114others(1): Show | 4 | HG00673.hp1 HG01952.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-4934G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987444 | ||||||
chr6:56987726
|
A | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-4652A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56987726 | ||||||
chr6:56988019
|
C | CT | 18 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0030others(15): Show | 19 | HG00408.hp2 HG00558.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.121-4344dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56988019 | |||||
chr6:56988019
|
CT | C | 45 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(42): Show | 56 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.121-4344delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56988019 | |||||
chr6:56988118
|
C | T | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4260C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988118 | ||||||
chr6:56988177
|
C | T | 50 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(47): Show | 61 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.121-4201C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988177 | ||||||
chr6:56988316
|
G | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-4062G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988316 | ||||||
chr6:56988433
|
A | G | 1 | a0001c0001t0007g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121-3945A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988433 | ||||||
chr6:56988631
|
T | A | 1 | a0001c0001t0002g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.121-3747T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988631 | ||||||
chr6:56988707
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.121-3671T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988707 | ||||||
chr6:56988900
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.121-3478G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988900 | ||||||
chr6:56988902
|
G | A | 3 | a0001c0001t0004g0009a0001c0001t0004g0058a0001c0001t0004g0061 | 4 | NA18989.hp2 NA19066.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-3476G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988902 | ||||||
chr6:56988932
|
G | A | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.121-3446G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988932 | ||||||
chr6:56988942
|
G | A | 52 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(49): Show | 63 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.121-3436G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988942 | ||||||
chr6:56988979
|
C | T | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.121-3399C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56988979 | ||||||
chr6:56989124
|
ATATAT | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0075 | 3 | HG02615.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.121-3248_121-3244d others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56989124 | |||||
chr6:56989236
|
T | C | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.121-3142T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56989236 | ||||||
chr6:56989443
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.121-2935A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56989443 | ||||||
chr6:56989473
|
C | A | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.121-2905C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56989473 | ||||||
chr6:56989608
|
TC | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.121-2769delC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56989608 | ||||||
chr6:56989922
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121-2456G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56989922 | ||||||
chr6:56990055
|
A | C | 1 | a0001c0001t0002g0160 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.121-2323A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990055 | ||||||
chr6:56990111
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.121-2267A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990111 | ||||||
chr6:56990249
|
C | CT | 40 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0077others(37): Show | 47 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.121-2109dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56990249 | |||||
chr6:56990297
|
CTGTG | C | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.121-2076_121-2073d others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 56990297 | |||||
chr6:56990428
|
G | C | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.121-1950G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990428 | ||||||
chr6:56990594
|
C | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.121-1784C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990594 | ||||||
chr6:56990656
|
G | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 177 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.121-1722G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990656 | ||||||
chr6:56990826
|
C | T | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.121-1552C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990826 | ||||||
chr6:56990836
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121-1542T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990836 | ||||||
chr6:56990923
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.121-1455T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56990923 | ||||||
chr6:56991017
|
C | T | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-1361C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991017 | ||||||
chr6:56991378
|
T | G | 1 | a0001c0001t0005g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.121-1000T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991378 | ||||||
chr6:56991444
|
G | T | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-934G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991444 | ||||||
chr6:56991518
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.121-860C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991518 | ||||||
chr6:56991651
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.121-727G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991651 | ||||||
chr6:56991724
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0125others(2): Show | 5 | HG01358.hp2 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-654T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991724 | ||||||
chr6:56991792
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.121-586A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56991792 | ||||||
chr6:56992044
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.121-334C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56992044 | ||||||
chr6:56992263
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.121-115G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56992263 | ||||||
chr6:56992305
|
G | C | 1 | a0001c0001t0004g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-73G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 2/6 | chr6 | 56992305 | ||||||
chr6:56992867
|
A | C | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.298+312A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56992867 | ||||||
chr6:56992890
|
A | ATAT | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+336_298+338dup others(3): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56992890 | |||||
chr6:56992994
|
G | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0068others(9): Show | 12 | HG01358.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+439G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56992994 | ||||||
chr6:56993274
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.298+719T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56993274 | ||||||
chr6:56993582
|
A | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1027A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56993582 | ||||||
chr6:56993939
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18939.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.298+1384A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56993939 | ||||||
chr6:56994011
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.298+1456T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994011 | ||||||
chr6:56994185
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0125others(2): Show | 5 | HG01358.hp2 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1630C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994185 | ||||||
chr6:56994284
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.298+1729C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994284 | ||||||
chr6:56994286
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.298+1731C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994286 | ||||||
chr6:56994413
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.298+1858G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994413 | ||||||
chr6:56994457
|
C | CA | 14 | a0001c0001t0001g0027a0001c0001t0001g0088a0001c0001t0001g0090others(11): Show | 14 | HG01071.hp2 HG01358.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+1929dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56994457 | |||||
chr6:56994457
|
C | CAA | 75 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.298+1928_298+1929d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56994457 | |||||
chr6:56994457
|
C | CAAA | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(18): Show | 23 | HG00597.hp2 HG01074.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.298+1927_298+1929d others(5): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56994457 | |||||
chr6:56994457
|
CA | C | 36 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(33): Show | 47 | HG00438.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.298+1929delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56994457 | |||||
chr6:56994457
|
CAA | C | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1928_298+1929d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56994457 | |||||
chr6:56994486
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.298+1931G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994486 | ||||||
chr6:56994512
|
G | C | 1 | a0001c0001t0003g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298+1957G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994512 | ||||||
chr6:56994658
|
G | C | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+2103G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994658 | ||||||
chr6:56994766
|
A | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.298+2211A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994766 | ||||||
chr6:56994921
|
C | A | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.298+2366C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56994921 | ||||||
chr6:56995041
|
T | C | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.298+2486T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995041 | ||||||
chr6:56995151
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.298+2596T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995151 | ||||||
chr6:56995223
|
A | T | 17 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(14): Show | 21 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.298+2668A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995223 | ||||||
chr6:56995453
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.298+2898G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995453 | ||||||
chr6:56995467
|
C | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+2912C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995467 | ||||||
chr6:56995539
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.298+2984G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995539 | ||||||
chr6:56995563
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18939.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.298+3008C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995563 | ||||||
chr6:56995649
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298+3094A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995649 | ||||||
chr6:56995787
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298+3232C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995787 | ||||||
chr6:56995897
|
T | C | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+3342T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56995897 | ||||||
chr6:56996095
|
T | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298+3540T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56996095 | ||||||
chr6:56996319
|
T | C | 56 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.298+3764T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56996319 | ||||||
chr6:56996479
|
A | C | 4 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+3924A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56996479 | ||||||
chr6:56996820
|
T | C | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+4265T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56996820 | ||||||
chr6:56997512
|
C | G | 53 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(50): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.298+4957C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997512 | ||||||
chr6:56997615
|
G | A | 53 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(50): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.298+5060G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997615 | ||||||
chr6:56997637
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+5082T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997637 | ||||||
chr6:56997702
|
T | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 199 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.298+5147T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997702 | ||||||
chr6:56997703
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.298+5148G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997703 | ||||||
chr6:56997844
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.298+5289G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997844 | ||||||
chr6:56997869
|
A | T | 1 | a0001c0001t0002g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.298+5314A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997869 | ||||||
chr6:56997956
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.298+5401G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997956 | ||||||
chr6:56997981
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.298+5426C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56997981 | ||||||
chr6:56998007
|
A | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+5452A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998007 | ||||||
chr6:56998111
|
G | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+5556G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998111 | ||||||
chr6:56998132
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.298+5577G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998132 | ||||||
chr6:56998356
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.298+5801A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998356 | ||||||
chr6:56998380
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0008g0092 | 3 | HG01123.hp1 HG01433.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.298+5825C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998380 | ||||||
chr6:56998482
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0075 | 3 | HG02615.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298+5927G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998482 | ||||||
chr6:56998711
|
AT | A | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 176 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.298+6165delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56998711 | |||||
chr6:56998741
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.298+6186G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998741 | ||||||
chr6:56998752
|
C | CA | 6 | a0001c0001t0002g0068a0001c0001t0002g0157a0001c0001t0002g0159others(3): Show | 6 | HG00438.hp1 HG02027.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+6209dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 56998752 | |||||
chr6:56998989
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298+6434G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56998989 | ||||||
chr6:56999087
|
T | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017 | 3 | HG02818.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.298+6532T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999087 | ||||||
chr6:56999131
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.298+6576A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999131 | ||||||
chr6:56999286
|
T | C | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+6731T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999286 | ||||||
chr6:56999457
|
A | C | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.298+6902A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999457 | ||||||
chr6:56999458
|
G | C | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.298+6903G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999458 | ||||||
chr6:56999758
|
C | T | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.298+7203C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999758 | ||||||
chr6:56999833
|
G | A | 56 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.298+7278G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999833 | ||||||
chr6:56999870
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0107 | 2 | HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.298+7315C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999870 | ||||||
chr6:56999895
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+7340C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999895 | ||||||
chr6:56999915
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.298+7360G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999915 | ||||||
chr6:56999939
|
T | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 199 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.298+7384T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 56999939 | ||||||
chr6:57000006
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0137a0001c0001t0002g0066others(1): Show | 4 | HG01433.hp2 HG01884.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+7451G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000006 | ||||||
chr6:57000057
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.298+7502G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000057 | ||||||
chr6:57000062
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+7507G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000062 | ||||||
chr6:57000106
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.298+7551G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000106 | ||||||
chr6:57000410
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.298+7855C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000410 | ||||||
chr6:57000581
|
AC | A | 35 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(32): Show | 42 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.298+8027delC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000581 | ||||||
chr6:57000582
|
C | A | 1 | a0001c0001t0002g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298+8027C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000582 | ||||||
chr6:57000586
|
CA | C | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+8043delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000586 | |||||
chr6:57000590
|
A | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.298+8035A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000590 | ||||||
chr6:57000591
|
A | C | 1 | a0001c0001t0004g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.298+8036A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000591 | ||||||
chr6:57000633
|
G | GA | 7 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(4): Show | 7 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+8093dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000633 | |||||
chr6:57000633
|
GA | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0077others(36): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.298+8093delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000633 | |||||
chr6:57000633
|
GAA | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+8092_298+8093d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000633 | |||||
chr6:57000884
|
G | GA | 11 | a0001c0001t0001g0024a0001c0001t0001g0102a0001c0001t0001g0103others(8): Show | 11 | HG02027.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+8347dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000884 | |||||
chr6:57000884
|
G | GAA | 5 | a0001c0001t0001g0088a0001c0001t0002g0070a0001c0001t0002g0125others(2): Show | 5 | HG01358.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+8346_298+8347d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000884 | |||||
chr6:57000884
|
GA | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0025others(71): Show | 83 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.298+8347delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57000884 | |||||
chr6:57000885
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.298+8330A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000885 | ||||||
chr6:57000903
|
G | C | 1 | a0001c0001t0003g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.298+8348G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57000903 | ||||||
chr6:57001003
|
A | C | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+8448A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001003 | ||||||
chr6:57001054
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298+8499G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001054 | ||||||
chr6:57001134
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.298+8579G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001134 | ||||||
chr6:57001155
|
CT | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 121 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.298+8617delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57001155 | |||||
chr6:57001155
|
CTT | C | 42 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(39): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.298+8616_298+8617d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57001155 | |||||
chr6:57001155
|
CTTT | C | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+8615_298+8617d others(5): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57001155 | |||||
chr6:57001158
|
T | A | 1 | a0001c0001t0002g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.298+8603T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001158 | ||||||
chr6:57001186
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.298+8631C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001186 | ||||||
chr6:57001263
|
A | T | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.298+8708A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001263 | ||||||
chr6:57001283
|
T | A | 48 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 59 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.298+8728T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001283 | ||||||
chr6:57001296
|
C | T | 56 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.298+8741C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001296 | ||||||
chr6:57001459
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.298+8904G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001459 | ||||||
chr6:57001870
|
G | T | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+9315G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57001870 | ||||||
chr6:57002052
|
G | A | 10 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+9497G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002052 | ||||||
chr6:57002239
|
C | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+9684C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002239 | ||||||
chr6:57002310
|
GC | G | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.298+9756delC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002310 | ||||||
chr6:57002524
|
C | A | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.298+9969C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002524 | ||||||
chr6:57002608
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.298+10053A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002608 | ||||||
chr6:57002613
|
C | CTT | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 202 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.298+10059_298+1006 others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57002613 | |||||
chr6:57002643
|
T | G | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.298+10088T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002643 | ||||||
chr6:57002665
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0002t0002g0133 | 3 | HG01884.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.298+10110T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002665 | ||||||
chr6:57002817
|
CA | C | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+10265delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57002817 | |||||
chr6:57002917
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.298+10362T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57002917 | ||||||
chr6:57003098
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.298+10543A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003098 | ||||||
chr6:57003127
|
AAC | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.298+10579_298+1058 others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57003127 | |||||
chr6:57003512
|
G | GCAA | 18 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0002g0015others(15): Show | 18 | HG02055.hp1 HG02132.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+10985_298+1098 others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57003512 | |||||
chr6:57003512
|
GCAACAA | G | 3 | a0001c0001t0001g0101a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01884.hp2 HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.298+10982_298+1098 others(10): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57003512 | |||||
chr6:57003543
|
A | C | 35 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(32): Show | 42 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.298+10988A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003543 | ||||||
chr6:57003781
|
AC | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+11227delC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003781 | ||||||
chr6:57003812
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+11257C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003812 | ||||||
chr6:57003949
|
T | C | 59 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(56): Show | 70 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.299-11184T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003949 | ||||||
chr6:57003954
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.299-11179A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57003954 | ||||||
chr6:57004000
|
C | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-11133C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004000 | ||||||
chr6:57004069
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0043 | 3 | HG00639.hp2 HG00733.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.299-11064T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004069 | ||||||
chr6:57004105
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.299-11028G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004105 | ||||||
chr6:57004332
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-10801T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004332 | ||||||
chr6:57004631
|
G | A | 12 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(9): Show | 16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-10502G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004631 | ||||||
chr6:57004874
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-10259A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57004874 | ||||||
chr6:57005321
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-9812G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005321 | ||||||
chr6:57005605
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0068others(4): Show | 7 | HG01358.hp2 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-9528G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005605 | ||||||
chr6:57005651
|
C | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.299-9482C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005651 | ||||||
chr6:57005675
|
A | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-9458A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005675 | ||||||
chr6:57005766
|
CAATTA | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0002g0068others(4): Show | 7 | HG01358.hp2 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-9364_299-9360d others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57005766 | |||||
chr6:57005769
|
T | A | 1 | a0001c0001t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.299-9364T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005769 | ||||||
chr6:57005869
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.299-9264C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57005869 | ||||||
chr6:57006156
|
AT | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0086 | 4 | HG03471.hp1 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-8971delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57006156 | |||||
chr6:57006291
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.299-8842C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57006291 | ||||||
chr6:57006499
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.299-8634G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57006499 | ||||||
chr6:57006646
|
A | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-8487A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57006646 | ||||||
chr6:57007049
|
G | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-8084G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57007049 | ||||||
chr6:57007060
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.299-8073T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57007060 | ||||||
chr6:57007392
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299-7741T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57007392 | ||||||
chr6:57007409
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-7724A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57007409 | ||||||
chr6:57007411
|
AC | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-7718delC | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57007411 | |||||
chr6:57007737
|
A | T | 1 | a0001c0001t0004g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299-7396A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57007737 | ||||||
chr6:57008034
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.299-7099G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008034 | ||||||
chr6:57008247
|
A | C | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.299-6886A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008247 | ||||||
chr6:57008271
|
T | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 199 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.299-6862T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008271 | ||||||
chr6:57008420
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-6713C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008420 | ||||||
chr6:57008553
|
C | T | 49 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(46): Show | 56 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.299-6580C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008553 | ||||||
chr6:57008624
|
G | A | 61 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(58): Show | 72 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.299-6509G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008624 | ||||||
chr6:57008650
|
A | G | 11 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(8): Show | 11 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-6483A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008650 | ||||||
chr6:57008676
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-6457G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008676 | ||||||
chr6:57008853
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-6280G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008853 | ||||||
chr6:57008905
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.299-6228T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57008905 | ||||||
chr6:57009060
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-6073C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009060 | ||||||
chr6:57009089
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-6044A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009089 | ||||||
chr6:57009136
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-5997G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009136 | ||||||
chr6:57009233
|
C | T | 36 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(33): Show | 43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.299-5900C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009233 | ||||||
chr6:57009325
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.299-5808G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009325 | ||||||
chr6:57009357
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.299-5776C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009357 | ||||||
chr6:57009737
|
G | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 202 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.299-5396G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009737 | ||||||
chr6:57009943
|
C | G | 1 | a0001c0001t0002g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-5190C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009943 | ||||||
chr6:57009959
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.299-5174C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57009959 | ||||||
chr6:57009989
|
T | TGAA | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 189 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.299-5140_299-5138d others(5): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57009989 | |||||
chr6:57010126
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299-5007A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57010126 | ||||||
chr6:57010135
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | NA18939.hp2 NA18984.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.299-4998C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57010135 | ||||||
chr6:57010893
|
C | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.299-4240C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57010893 | ||||||
chr6:57010991
|
T | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-4142T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57010991 | ||||||
chr6:57011187
|
A | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-3946A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011187 | ||||||
chr6:57011243
|
G | A | 61 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(58): Show | 72 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.299-3890G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011243 | ||||||
chr6:57011294
|
C | T | 11 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(8): Show | 11 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-3839C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011294 | ||||||
chr6:57011364
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-3769A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011364 | ||||||
chr6:57011389
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.299-3744A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011389 | ||||||
chr6:57011427
|
T | C | 5 | a0001c0001t0002g0069a0001c0001t0002g0071a0001c0001t0002g0072others(2): Show | 5 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-3706T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011427 | ||||||
chr6:57011433
|
T | C | 31 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.299-3700T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011433 | ||||||
chr6:57011508
|
A | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-3625A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011508 | ||||||
chr6:57011574
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.299-3559C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011574 | ||||||
chr6:57011715
|
C | CA | 15 | a0001c0001t0001g0026a0001c0001t0001g0107a0001c0001t0002g0015others(12): Show | 15 | HG02040.hp2 HG02055.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-3398dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57011715 | |||||
chr6:57011715
|
C | CAA | 27 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(24): Show | 34 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.299-3399_299-3398d others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57011715 | |||||
chr6:57011731
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.299-3402A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57011731 | ||||||
chr6:57011758
|
A | AAAAG | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-3359_299-3356d others(6): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57011758 | |||||
chr6:57011770
|
GAAAGA | G | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-3354_299-3350d others(7): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57011770 | |||||
chr6:57012074
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-3059G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012074 | ||||||
chr6:57012156
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-2977G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012156 | ||||||
chr6:57012210
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.299-2923A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012210 | ||||||
chr6:57012491
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.299-2642T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012491 | ||||||
chr6:57012507
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-2626A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012507 | ||||||
chr6:57012508
|
T | C | 8 | a0001c0001t0002g0014a0001c0001t0002g0144a0001c0001t0002g0157others(5): Show | 9 | HG00438.hp1 HG00558.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-2625T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012508 | ||||||
chr6:57012520
|
A | G | 11 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(8): Show | 15 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-2613A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012520 | ||||||
chr6:57012533
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-2600A>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012533 | ||||||
chr6:57012662
|
G | A | 62 | a0001c0001t0001g0077a0001c0001t0001g0135a0001c0001t0002g0001others(59): Show | 73 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.299-2471G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012662 | ||||||
chr6:57012675
|
T | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 202 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.299-2458T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012675 | ||||||
chr6:57012699
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-2434A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012699 | ||||||
chr6:57012718
|
AG | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-2414delG | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012718 | ||||||
chr6:57012719
|
G | A | 31 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0003others(28): Show | 38 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.299-2414G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012719 | ||||||
chr6:57012807
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.299-2326A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57012807 | ||||||
chr6:57012966
|
C | CT | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-2165dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57012966 | |||||
chr6:57013040
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0116 | 2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.299-2093C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57013040 | ||||||
chr6:57013426
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-1707C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57013426 | ||||||
chr6:57013475
|
T | A | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-1658T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57013475 | ||||||
chr6:57013599
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.299-1534C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57013599 | ||||||
chr6:57013953
|
C | T | 5 | a0001c0001t0002g0069a0001c0001t0002g0071a0001c0001t0002g0072others(2): Show | 5 | HG02451.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1180C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57013953 | ||||||
chr6:57014830
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.299-303C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57014830 | ||||||
chr6:57015014
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.299-119A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57015014 | ||||||
chr6:57015026
|
A | AAC | 50 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0107others(47): Show | 57 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.299-106_299-105ins others(2): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57015026 | |||||
chr6:57015037
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-96G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57015037 | ||||||
chr6:57015063
|
C | CA | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-63dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 57015063 | |||||
chr6:57015073
|
T | C | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-60T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57015073 | ||||||
chr6:57015095
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.299-38A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 3/6 | chr6 | 57015095 | ||||||
chr6:57015528
|
T | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.519+175T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015528 | ||||||
chr6:57015539
|
C | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.519+186C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015539 | ||||||
chr6:57015641
|
C | CA | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0115others(2): Show | 5 | HG01891.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+302dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 57015641 | |||||
chr6:57015641
|
CA | C | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+302delA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 57015641 | |||||
chr6:57015661
|
C | T | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+308C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015661 | ||||||
chr6:57015664
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.519+311A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015664 | ||||||
chr6:57015676
|
G | A | 8 | a0001c0001t0004g0009a0001c0001t0004g0057a0001c0001t0004g0058others(5): Show | 9 | NA18943.hp1 NA18989.hp2 NA19000.hp1 others(6): Show |
intron_variant | MODIFIER | c.519+323G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015676 | ||||||
chr6:57015842
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.519+489C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57015842 | ||||||
chr6:57016173
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.519+820T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57016173 | ||||||
chr6:57016539
|
G | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(6): Show | 10 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-668G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57016539 | ||||||
chr6:57016700
|
C | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.520-507C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57016700 | ||||||
chr6:57016836
|
T | C | 7 | a0001c0001t0002g0014a0001c0001t0002g0157a0001c0001t0002g0159others(4): Show | 8 | HG00438.hp1 HG00558.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-371T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57016836 | ||||||
chr6:57017085
|
A | G | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-122A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57017085 | ||||||
chr6:57017118
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.520-89G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 4/6 | chr6 | 57017118 | ||||||
chr6:57017696
|
A | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 106 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.712+297A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57017696 | ||||||
chr6:57017851
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.712+452G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57017851 | ||||||
chr6:57018077
|
ATCAG | A | 32 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0107others(29): Show | 39 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.713-339_713-336del others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 57018077 | |||||
chr6:57018197
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0075 | 3 | HG02615.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.713-224C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018197 | ||||||
chr6:57018228
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.713-193T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018228 | ||||||
chr6:57018233
|
T | G | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.713-188T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018233 | ||||||
chr6:57018331
|
T | G | 1 | a0001c0001t0002g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.713-90T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018331 | ||||||
chr6:57018370
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.713-51G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018370 | ||||||
chr6:57018398
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.713-23G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 5/6 | chr6 | 57018398 | ||||||
chr6:57018807
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0002g0021 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*9+250C>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57018807 | ||||||
chr6:57018946
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.*9+389T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57018946 | ||||||
chr6:57019106
|
T | C | 2 | a0001c0001t0003g0174a0001c0001t0003g0177 | 2 | HG01109.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.*9+549T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019106 | ||||||
chr6:57019281
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*9+724C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019281 | ||||||
chr6:57019352
|
A | G | 6 | a0001c0001t0001g0088a0001c0001t0002g0068a0001c0001t0002g0125others(3): Show | 6 | HG01358.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.*9+795A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019352 | ||||||
chr6:57019381
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*9+824G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019381 | ||||||
chr6:57019653
|
T | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.*9+1096T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019653 | ||||||
chr6:57019719
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 5 | HG01358.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.*9+1162A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019719 | ||||||
chr6:57019845
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.*9+1288A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57019845 | ||||||
chr6:57020080
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*9+1523C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020080 | ||||||
chr6:57020181
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.*9+1624A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020181 | ||||||
chr6:57020220
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 203 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.*9+1663T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020220 | ||||||
chr6:57020277
|
A | AT | 9 | a0001c0001t0001g0054a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.*9+1737dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57020277 | |||||
chr6:57020277
|
AT | A | 11 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0115others(8): Show | 11 | HG01358.hp2 HG02886.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.*9+1737delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57020277 | |||||
chr6:57020398
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*9+1841T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020398 | ||||||
chr6:57020553
|
T | C | 10 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(7): Show | 11 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(8): Show |
intron_variant | MODIFIER | c.*9+1996T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020553 | ||||||
chr6:57020567
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.*9+2010C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020567 | ||||||
chr6:57020702
|
G | A | 10 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(7): Show | 11 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(8): Show |
intron_variant | MODIFIER | c.*9+2145G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020702 | ||||||
chr6:57020752
|
C | G | 1 | a0001c0001t0003g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*9+2195C>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020752 | ||||||
chr6:57020833
|
G | GT | 27 | a0001c0001t0001g0088a0001c0001t0001g0135a0001c0001t0002g0015others(24): Show | 31 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.*9+2297dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57020833 | |||||
chr6:57020840
|
T | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.*9+2283T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020840 | ||||||
chr6:57020840
|
T | TG | 10 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0004g0009others(7): Show | 11 | HG01884.hp2 HG03195.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.*9+2283_*9+2284ins others(1): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020840 | ||||||
chr6:57020845
|
T | G | 2 | a0001c0001t0002g0153a0001c0001t0002g0162 | 2 | HG00597.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.*9+2288T>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020845 | ||||||
chr6:57020845
|
T | TG | 29 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0107others(26): Show | 36 | HG00438.hp1 HG00558.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.*9+2288_*9+2289ins others(1): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57020845 | ||||||
chr6:57021232
|
GAC | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.*9+2677_*9+2678del others(2): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57021232 | |||||
chr6:57021352
|
C | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*9+2795C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021352 | ||||||
chr6:57021374
|
T | C | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*9+2817T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021374 | ||||||
chr6:57021389
|
A | G | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.*9+2832A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021389 | ||||||
chr6:57021482
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0098 | 2 | NA18939.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.*9+2925T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021482 | ||||||
chr6:57021538
|
A | C | 49 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0077others(46): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.*9+2981A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021538 | ||||||
chr6:57021538
|
A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.*9+2981A>G | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021538 | ||||||
chr6:57021751
|
G | A | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*9+3194G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021751 | ||||||
chr6:57021848
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*9+3291G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021848 | ||||||
chr6:57021884
|
G | A | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*9+3327G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021884 | ||||||
chr6:57021949
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0135a0001c0001t0002g0021others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.*9+3392G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57021949 | ||||||
chr6:57022048
|
C | T | 26 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0107others(23): Show | 32 | HG00597.hp1 HG00673.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.*9+3491C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022048 | ||||||
chr6:57022144
|
ATTTTTCT others(1): Show |
A | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.*9+3599_*9+3606del others(8): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57022144 | |||||
chr6:57022158
|
CTTTT | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0076 | 3 | HG03471.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*9+3603_*9+3606del others(4): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57022158 | |||||
chr6:57022164
|
C | CT | 17 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0050others(14): Show | 17 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.*9+3625dupT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57022164 | |||||
chr6:57022164
|
CT | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0110a0001c0001t0001g0124others(13): Show | 16 | HG01099.hp2 HG01496.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.*9+3625delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57022164 | |||||
chr6:57022167
|
T | TC | 2 | a0001c0001t0001g0026a0001c0001t0002g0154 | 2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.*9+3610_*9+3611ins others(1): Show |
BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022167 | ||||||
chr6:57022168
|
T | C | 23 | a0001c0001t0001g0077a0001c0001t0001g0107a0001c0001t0002g0001others(20): Show | 29 | HG00597.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.*9+3611T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022168 | ||||||
chr6:57022169
|
T | C | 2 | a0001c0001t0002g0148a0001c0001t0002g0150 | 2 | HG01099.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.*9+3612T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022169 | ||||||
chr6:57022463
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0135a0001c0001t0002g0021 | 3 | HG02258.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.*10-3619G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022463 | ||||||
chr6:57022512
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0124 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.*10-3570C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022512 | ||||||
chr6:57022574
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0135a0001c0001t0002g0021others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.*10-3508T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57022574 | ||||||
chr6:57022747
|
CT | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 58 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.*10-3329delT | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57022747 | |||||
chr6:57023540
|
TG | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0135a0001c0001t0002g0021others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.*10-2540delG | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57023540 | |||||
chr6:57023579
|
T | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0129 | 2 | HG04115.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*10-2503T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57023579 | ||||||
chr6:57023709
|
G | A | 25 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0107others(22): Show | 31 | HG00597.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.*10-2373G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57023709 | ||||||
chr6:57023748
|
G | A | 1 | a0001c0001t0007g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*10-2334G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57023748 | ||||||
chr6:57023848
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.*10-2234T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57023848 | ||||||
chr6:57023866
|
T | C | 1 | a0001c0001t0006g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*10-2216T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57023866 | ||||||
chr6:57024062
|
T | TA | 10 | a0001c0001t0004g0009a0001c0001t0004g0056a0001c0001t0004g0057others(7): Show | 11 | HG02132.hp1 NA18943.hp1 NA18989.hp2 others(8): Show |
intron_variant | MODIFIER | c.*10-2013dupA | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 57024062 | |||||
chr6:57024097
|
G | C | 1 | a0001c0001t0002g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*10-1985G>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024097 | ||||||
chr6:57024528
|
T | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0128 | 2 | HG01358.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*10-1554T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024528 | ||||||
chr6:57024587
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*10-1495T>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024587 | ||||||
chr6:57024762
|
G | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 203 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.*10-1320G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024762 | ||||||
chr6:57024800
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0076 | 3 | HG03471.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*10-1282C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024800 | ||||||
chr6:57024963
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.*10-1119G>A | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57024963 | ||||||
chr6:57025140
|
A | C | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02976.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.*10-942A>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025140 | ||||||
chr6:57025285
|
T | C | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.*10-797T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025285 | ||||||
chr6:57025675
|
T | C | 1 | a0001c0001t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*10-407T>C | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025675 | ||||||
chr6:57025841
|
C | T | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 192 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.*10-241C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025841 | ||||||
chr6:57025900
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*10-182C>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025900 | ||||||
chr6:57025917
|
G | T | 1 | a0001c0001t0009g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*10-165G>T | BEND6 | ENSG00000151917.18 | transcript | ENST00000370746.8 | protein_coding | 6/6 | chr6 | 57025917 |