Item | Value |
---|---|
geneid | 51666 |
ensemblid | ENSG00000005981.13 |
hgncid | 16009 |
symbol | ASB4 |
name | ankyrin repeat and SOCS box containing 4 |
refseq_nuc | NM_016116.3 |
refseq_prot | NP_057200.1 |
ensembl_nuc | ENST00000325885.6 |
ensembl_prot | ENSP00000321388.5 |
mane_status | MANE Select |
chr | chr7 |
start | 95485943 |
end | 95540233 |
strand | + |
ver | v1.2 |
region | chr7:95485943-95540233 |
region5000 | chr7:95480943-95545233 |
regionname0 | ASB4_chr7_95485943_95540233 |
regionname5000 | ASB4_chr7_95480943_95545233 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 426 | 371 | 84 | 76 | 149 | 14 | 46 | 109 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002 | 0/0 | 426 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0003 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0004 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0005 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1281 | 370 | 83 | 76 | 149 | 14 | 46 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
c0002 | 0/0 | 1281 | 14 | 13 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
c0003 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
c0004 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
c0005 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
c0006 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2502 | 197 | 10 | 35 | 115 | 7 | 29 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0002 | 0/0 | 2502 | 47 | 14 | 8 | 19 | 0 | 6 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0003 | 0/0 | 2504 | 40 | 11 | 16 | 6 | 3 | 4 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0004 | 0/0 | 2502 | 31 | 15 | 5 | 6 | 1 | 4 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0005 | 0/0 | 2502 | 13 | 13 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0006 | 0/0 | 2502 | 11 | 10 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0007 | 0/0 | 2501 | 6 | 6 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0008 | 1/0 | 2504 | 6 | 0 | 3 | 0 | 1 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0009 | 0/0 | 2502 | 5 | 5 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0010 | 0/0 | 2502 | 5 | 0 | 5 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0011 | 0/0 | 2503 | 4 | 4 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0012 | 0/0 | 2503 | 3 | 3 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0013 | 0/0 | 2502 | 3 | 0 | 3 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0014 | 0/0 | 2504 | 2 | 0 | 1 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0015 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0016 | 0/0 | 2504 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0017 | 0/0 | 2502 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0018 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0019 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0020 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0021 | 0/0 | 2503 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0022 | 0/0 | 2504 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0023 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0024 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
t0025 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0336 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1281 | 370 | 83 | 76 | 149 | 14 | 46 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
a0001c0006 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
a0002c0002 | 0/0 | 1281 | 14 | 13 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
a0003c0005 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
a0004c0004 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 | |
a0005c0003 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3782 | 195 | 9 | 34 | 115 | 7 | 29 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0002 | 0/0 | 3782 | 47 | 14 | 8 | 19 | 0 | 6 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0003 | 0/0 | 3784 | 38 | 9 | 16 | 6 | 3 | 4 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0004 | 0/0 | 3782 | 27 | 12 | 5 | 5 | 1 | 4 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0005 | 0/0 | 3782 | 13 | 13 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0006 | 0/0 | 3782 | 3 | 3 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0007 | 0/0 | 3781 | 6 | 6 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0008 | 1/0 | 3784 | 6 | 0 | 3 | 0 | 1 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0009 | 0/0 | 3782 | 5 | 5 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0010 | 0/0 | 3782 | 5 | 0 | 5 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0011 | 0/0 | 3783 | 4 | 4 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0012 | 0/0 | 3783 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0013 | 0/0 | 3782 | 3 | 0 | 3 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0014 | 0/0 | 3784 | 2 | 0 | 1 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0015 | 0/0 | 3782 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0016 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0017 | 0/0 | 3782 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0018 | 0/0 | 3782 | 2 | 2 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0019 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0020 | 0/0 | 3782 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0021 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0022 | 0/0 | 3784 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0023 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0024 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0001t0025 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0001c0006t0003 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002c0002t0001 | 0/0 | 3782 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002c0002t0003 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002c0002t0004 | 0/0 | 3782 | 3 | 3 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002c0002t0006 | 0/0 | 3782 | 8 | 7 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0002c0002t0012 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0003c0005t0001 | 0/0 | 3782 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0004c0004t0004 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
a0005c0003t0016 | 0/0 | 3784 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | copy fasta | chr7 | 95480943 | 95545233 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0336 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0005g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0007g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0010g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0010g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0012g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0012g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0013g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0013g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0013g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0014g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0016g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0017g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0017g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0018g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0018g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0019g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0020g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0021g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0022g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0023g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0001t0025g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0001c0006t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0006g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0002c0002t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0003c0005t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0004c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
a0005c0003t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0355 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0077 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0344 | EUR | FIN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00738 | hp2 | a0002 | c0002 | t0006 | g0372 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00741 | hp1 | a0003 | c0005 | t0001 | g0354 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0140 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0346 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0123 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0333 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01192 | hp1 | a0001 | c0001 | t0010 | g0182 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0341 | AMR | PUR | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0197 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01258 | hp1 | a0001 | c0001 | t0013 | g0195 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01261 | hp1 | a0001 | c0001 | t0014 | g0098 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0186 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01361 | hp2 | a0001 | c0001 | t0013 | g0196 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01433 | hp1 | a0001 | c0001 | t0010 | g0188 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0356 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0091 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01516 | hp1 | a0001 | c0001 | t0014 | g0104 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01516 | hp2 | a0001 | c0001 | t0008 | g0236 | EUR | IBS | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0318 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0079 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01975 | hp2 | a0001 | c0001 | t0010 | g0187 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02258 | hp2 | a0001 | c0006 | t0003 | g0238 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0260 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02293 | hp1 | a0001 | c0001 | t0020 | g0096 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02300 | hp1 | a0001 | c0001 | t0010 | g0185 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0037 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02572 | hp1 | a0002 | c0002 | t0003 | g0371 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0338 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02602 | hp2 | a0001 | c0001 | t0008 | g0165 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0376 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02717 | hp1 | a0005 | c0003 | t0016 | g0053 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02809 | hp1 | a0002 | c0002 | t0006 | g0034 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0378 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0339 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02886 | hp2 | a0002 | c0002 | t0012 | g0030 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02895 | hp1 | a0002 | c0002 | t0006 | g0031 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02897 | hp1 | a0002 | c0002 | t0006 | g0032 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0296 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0370 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02970 | hp1 | a0001 | c0001 | t0018 | g0310 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0288 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02976 | hp2 | a0002 | c0002 | t0006 | g0038 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0320 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03130 | hp1 | a0001 | c0001 | t0012 | g0379 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03130 | hp2 | a0002 | c0002 | t0006 | g0035 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03139 | hp2 | a0001 | c0001 | t0021 | g0018 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0250 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0375 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0041 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0282 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | ESN | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03579 | hp2 | a0002 | c0002 | t0006 | g0033 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04115 | hp1 | a0001 | c0001 | t0017 | g0291 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0359 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0302 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18953 | hp2 | a0001 | c0001 | t0019 | g0171 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18959 | hp2 | a0004 | c0004 | t0004 | g0105 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18966 | hp1 | a0001 | c0001 | t0024 | g0211 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18972 | hp2 | a0001 | c0001 | t0025 | g0268 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19002 | hp1 | a0001 | c0001 | t0023 | g0218 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0377 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0374 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19043 | hp1 | a0002 | c0002 | t0004 | g0028 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA19240 | hp2 | a0001 | c0001 | t0015 | g0113 | AFR | YRI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ASW | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ASW | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20752 | hp1 | a0001 | c0001 | t0022 | g0071 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | TSI | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | GIH | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | GIH | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0029 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | ACB | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0036 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | MSL | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0380 | AFR | LWK | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0336 | REF | REF | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0080 | REF | REF | ASB4_chr7_95480943_95545233 | ASB4 | chr7 | 95480943 | 95545233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:95486020 | G | C | 1 | a0002 | 14 | HG00738.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.49G>C | p.Val17Leu | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/5 | 78/3784 | 49/1281 | 17/426 | chr7 | 95486020 | ||
chr7:95486062 | G | A | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.91G>A | p.Gly31Arg | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/5 | 120/3784 | 91/1281 | 31/426 | chr7 | 95486062 | ||
chr7:95528113 | G | C | 1 | a0004 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.788G>C | p.Cys263Ser | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/5 | 817/3784 | 788/1281 | 263/426 | chr7 | 95528113 | ||
chr7:95536518 | T | C | 1 | a0003 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1060T>C | p.Trp354Arg | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/5 | 1089/3784 | 1060/1281 | 354/426 | chr7 | 95536518 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:95536448 | C | T | 1 | a0001c0006 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.990C>T | p.Ala330Ala | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/5 | 1019/3784 | 990/1281 | 330/426 | chr7 | 95536448 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:95537892 | C | T | 9 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(6): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 133 | chr7 | 95537892 | |||||
chr7:95538122 | T | C | 3 | a0001c0001t0002a0001c0001t0014a0001c0001t0019 | 50 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*363T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 363 | chr7 | 95538122 | |||||
chr7:95538191 | C | A | 1 | a0001c0001t0010 | 5 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 432 | chr7 | 95538191 | |||||
chr7:95538231 | G | A | 8 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(5): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*472G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 472 | chr7 | 95538231 | |||||
chr7:95538256 | C | T | 1 | a0001c0001t0013 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*497C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 497 | chr7 | 95538256 | |||||
chr7:95538669 | A | C | 1 | a0001c0001t0009 | 5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*910A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 910 | chr7 | 95538669 | |||||
chr7:95538818 | T | C | 1 | a0001c0001t0017 | 2 | HG03490.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1059 | chr7 | 95538818 | |||||
chr7:95538828 | C | T | 1 | a0001c0001t0022 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1069 | chr7 | 95538828 | |||||
chr7:95538909 | C | T | 2 | a0001c0001t0012a0002c0002t0012 | 3 | HG02818.hp1 HG02886.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1150C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1150 | chr7 | 95538909 | |||||
chr7:95538910 | G | A | 1 | a0001c0001t0015 | 2 | HG01884.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1151G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1151 | chr7 | 95538910 | |||||
chr7:95539067 | C | CT | 4 | a0001c0001t0011a0001c0001t0012a0001c0001t0021others(1): Show | 8 | HG02647.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1318dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1319 | INFO_REALIGN_3_PRIME | chr7 | 95539067 | ||||
chr7:95539084 | GCT | G | 1 | a0001c0001t0005 | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1326_*1327delCT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1326 | chr7 | 95539084 | |||||
chr7:95539085 | CTA | C | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1329_*1330delTA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1329 | INFO_REALIGN_3_PRIME | chr7 | 95539085 | ||||
chr7:95539087 | A | T | 1 | a0001c0001t0005 | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1328A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1328 | chr7 | 95539087 | |||||
chr7:95539144 | G | A | 1 | a0001c0001t0019 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1385G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1385 | chr7 | 95539144 | |||||
chr7:95539249 | G | A | 1 | a0001c0001t0023 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1490G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1490 | chr7 | 95539249 | |||||
chr7:95539523 | G | T | 1 | a0001c0001t0009 | 5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1764 | chr7 | 95539523 | |||||
chr7:95539664 | T | C | 1 | a0001c0001t0021 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1905T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 1905 | chr7 | 95539664 | |||||
chr7:95539815 | A | T | 2 | a0001c0001t0006a0002c0002t0006 | 11 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2056A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2056 | chr7 | 95539815 | |||||
chr7:95539959 | T | C | 2 | a0001c0001t0016a0005c0003t0016 | 2 | HG02717.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2200T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2200 | chr7 | 95539959 | |||||
chr7:95540053 | C | T | 1 | a0001c0001t0025 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2294C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2294 | chr7 | 95540053 | |||||
chr7:95540070 | AC | A | 1 | a0001c0001t0007 | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2312delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2312 | chr7 | 95540070 | |||||
chr7:95540078 | T | A | 1 | a0001c0001t0020 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2319 | chr7 | 95540078 | |||||
chr7:95540102 | A | T | 1 | a0001c0001t0024 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2343A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2343 | chr7 | 95540102 | |||||
chr7:95540202 | G | T | 7 | a0001c0001t0003a0001c0001t0014a0001c0001t0016others(4): Show | 45 | HG00323.hp1 HG01070.hp1 HG01109.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2443G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 5/5 | 2443 | chr7 | 95540202 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:95486187 | CT | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(6): Show | 9 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+30delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486187 | ||||||
chr7:95486204 | A | T | 7 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+46A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486204 | ||||||
chr7:95486267 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.187+109C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486267 | ||||||
chr7:95486334 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.187+176T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486334 | ||||||
chr7:95486336 | T | C | 12 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0022others(9): Show | 12 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+178T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486336 | ||||||
chr7:95486348 | G | A | 5 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+190G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486348 | ||||||
chr7:95486375 | TG | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(6): Show | 9 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+220delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95486375 | |||||
chr7:95486650 | C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(52): Show | 57 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.187+492C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486650 | ||||||
chr7:95486661 | G | T | 3 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0015g0318 | 3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.187+503G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486661 | ||||||
chr7:95486673 | T | C | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+515T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486673 | ||||||
chr7:95486756 | C | A | 12 | a0002c0002t0001g0039a0002c0002t0004g0028a0002c0002t0004g0029others(9): Show | 12 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+598C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486756 | ||||||
chr7:95486832 | G | A | 2 | a0002c0002t0004g0028a0002c0002t0004g0029 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.187+674G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486832 | ||||||
chr7:95486865 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.187+707A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95486865 | ||||||
chr7:95487053 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.187+895C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487053 | ||||||
chr7:95487192 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+1034A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487192 | ||||||
chr7:95487342 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.187+1184A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487342 | ||||||
chr7:95487403 | AAACT | A | 5 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(2): Show | 5 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1248_187+1251d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95487403 | |||||
chr7:95487520 | T | G | 7 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+1362T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487520 | ||||||
chr7:95487565 | A | T | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0037others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+1407A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487565 | ||||||
chr7:95487709 | T | C | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1551T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487709 | ||||||
chr7:95487794 | G | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1636G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487794 | ||||||
chr7:95487829 | A | C | 2 | a0001c0001t0003g0309a0001c0001t0018g0310 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.187+1671A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95487829 | ||||||
chr7:95488157 | C | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1999C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488157 | ||||||
chr7:95488191 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+2033A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488191 | ||||||
chr7:95488251 | G | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(114): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.187+2093G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488251 | ||||||
chr7:95488254 | T | C | 13 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(10): Show | 13 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+2096T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488254 | ||||||
chr7:95488294 | T | C | 1 | a0001c0001t0021g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.187+2136T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488294 | ||||||
chr7:95488346 | GA | G | 314 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(311): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.187+2199delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95488346 | |||||
chr7:95488391 | A | G | 349 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(346): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.187+2233A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488391 | ||||||
chr7:95488506 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.187+2348T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488506 | ||||||
chr7:95488531 | T | C | 3 | a0001c0001t0002g0111a0001c0001t0003g0112a0001c0001t0015g0113 | 3 | HG03471.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.187+2373T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488531 | ||||||
chr7:95488675 | G | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0040others(197): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.187+2517G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488675 | ||||||
chr7:95488754 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.187+2596T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488754 | ||||||
chr7:95488774 | C | G | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG00738.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+2616C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488774 | ||||||
chr7:95488804 | C | G | 117 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(114): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.187+2646C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488804 | ||||||
chr7:95488885 | A | C | 5 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(2): Show | 5 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2727A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488885 | ||||||
chr7:95488904 | A | G | 1 | a0002c0002t0006g0372 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.187+2746A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95488904 | ||||||
chr7:95489052 | G | C | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+2894G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489052 | ||||||
chr7:95489279 | G | A | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+3121G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489279 | ||||||
chr7:95489283 | T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(69): Show | 74 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.187+3125T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489283 | ||||||
chr7:95489375 | A | C | 1 | a0001c0001t0009g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.187+3217A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489375 | ||||||
chr7:95489407 | A | G | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0037others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+3249A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489407 | ||||||
chr7:95489433 | C | G | 1 | a0001c0001t0003g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3275C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489433 | ||||||
chr7:95489516 | G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(84): Show | 91 | HG00423.hp1 HG00609.hp2 HG01081.hp2 others(88): Show |
intron_variant | MODIFIER | c.187+3358G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489516 | ||||||
chr7:95489698 | C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(52): Show | 57 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.187+3540C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489698 | ||||||
chr7:95489760 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.187+3602C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489760 | ||||||
chr7:95489831 | A | G | 2 | a0001c0001t0004g0319a0001c0001t0004g0320 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.187+3673A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489831 | ||||||
chr7:95489898 | G | C | 313 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.187+3740G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489898 | ||||||
chr7:95489931 | G | C | 1 | a0002c0002t0012g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.187+3773G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489931 | ||||||
chr7:95489949 | T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0040others(197): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.187+3791T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95489949 | ||||||
chr7:95490066 | T | G | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+3908T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490066 | ||||||
chr7:95490283 | T | C | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+4125T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490283 | ||||||
chr7:95490343 | C | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(77): Show | 84 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.187+4185C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490343 | ||||||
chr7:95490366 | A | C | 1 | a0001c0001t0002g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+4208A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490366 | ||||||
chr7:95490719 | C | T | 1 | a0001c0001t0005g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+4561C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490719 | ||||||
chr7:95490815 | C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+4657C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490815 | ||||||
chr7:95490818 | A | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+4660A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490818 | ||||||
chr7:95490835 | C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(104): Show | 111 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(108): Show |
intron_variant | MODIFIER | c.187+4677C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490835 | ||||||
chr7:95490939 | C | T | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(18): Show | 21 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.187+4781C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490939 | ||||||
chr7:95490950 | C | A | 7 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+4792C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490950 | ||||||
chr7:95490950 | C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(7): Show | 10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+4792C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95490950 | ||||||
chr7:95491112 | T | A | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-4646T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491112 | ||||||
chr7:95491242 | ATC | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-4512_188-4511d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95491242 | |||||
chr7:95491324 | C | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(88): Show | 95 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-4434C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491324 | ||||||
chr7:95491334 | G | T | 1 | a0005c0003t0016g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-4424G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491334 | ||||||
chr7:95491412 | C | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(118): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.188-4346C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491412 | ||||||
chr7:95491707 | T | C | 311 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.188-4051T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491707 | ||||||
chr7:95491900 | C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0181others(60): Show | 65 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.188-3858C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491900 | ||||||
chr7:95491933 | C | A | 3 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0015g0318 | 3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-3825C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95491933 | ||||||
chr7:95492248 | C | T | 3 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0015g0318 | 3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-3510C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492248 | ||||||
chr7:95492260 | G | A | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.188-3498G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492260 | ||||||
chr7:95492299 | A | C | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-3459A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492299 | ||||||
chr7:95492334 | A | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-3424A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492334 | ||||||
chr7:95492454 | T | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(18): Show | 21 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.188-3304T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492454 | ||||||
chr7:95492596 | T | C | 3 | a0001c0001t0013g0195a0001c0001t0013g0196a0001c0001t0013g0197 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.188-3162T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492596 | ||||||
chr7:95492675 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188-3083C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492675 | ||||||
chr7:95492690 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.188-3068C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95492690 | ||||||
chr7:95493328 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.188-2430C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493328 | ||||||
chr7:95493361 | A | AGT | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG00639.hp1 HG01928.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-2368_188-2367d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493361 | A | AGTGTGT | 3 | a0001c0001t0005g0024a0001c0001t0005g0025a0001c0001t0005g0026 | 3 | HG02055.hp1 HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.188-2372_188-2367d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493361 | AGT | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(7): Show | 10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-2368_188-2367d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493361 | AGTGT | A | 7 | a0001c0001t0001g0087a0001c0001t0002g0177a0001c0001t0004g0085others(4): Show | 7 | HG00735.hp2 HG01346.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-2370_188-2367d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493361 | AGTGTGT | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0124others(86): Show | 93 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(90): Show |
intron_variant | MODIFIER | c.188-2372_188-2367d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493361 | AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0001g0116a0001c0001t0001g0178a0001c0001t0001g0311others(5): Show | 8 | HG01261.hp2 HG01934.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-2374_188-2367d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493361 | |||||
chr7:95493374 | GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02083.hp1 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.188-2368_188-2351d others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493374 | |||||
chr7:95493378 | GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18959.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.188-2366_188-2353d others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493378 | |||||
chr7:95493380 | GTGTGTGT others(5): Show |
G | 52 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(49): Show | 53 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.188-2366_188-2355d others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493380 | |||||
chr7:95493382 | GTGTGTGT others(3): Show |
G | 23 | a0001c0001t0001g0006a0001c0001t0001g0249a0001c0001t0001g0252others(20): Show | 24 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-2366_188-2357d others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493382 | |||||
chr7:95493384 | GTGTGTGT others(1): Show |
G | 90 | a0001c0001t0001g0007a0001c0001t0001g0256a0001c0001t0001g0263others(87): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.188-2366_188-2359d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493384 | |||||
chr7:95493386 | GTGTGTA | G | 3 | a0001c0001t0016g0370a0002c0002t0003g0371a0002c0002t0006g0372 | 3 | HG00738.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.188-2366_188-2361d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493386 | |||||
chr7:95493388 | G | A | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2370G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493388 | ||||||
chr7:95493390 | GTA | G | 17 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(14): Show | 17 | HG01081.hp2 HG01192.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-2366_188-2365d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95493390 | |||||
chr7:95493392 | A | G | 9 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(6): Show | 9 | HG00639.hp1 HG01358.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-2366A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493392 | ||||||
chr7:95493595 | A | G | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG00609.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.188-2163A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493595 | ||||||
chr7:95493670 | C | T | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2088C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493670 | ||||||
chr7:95493866 | T | A | 1 | a0001c0001t0001g0336 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.188-1892T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493866 | ||||||
chr7:95493876 | A | G | 30 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0049others(27): Show | 30 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.188-1882A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493876 | ||||||
chr7:95493891 | C | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(121): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.188-1867C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493891 | ||||||
chr7:95493892 | G | A | 2 | a0002c0002t0006g0031a0002c0002t0006g0032 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.188-1866G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493892 | ||||||
chr7:95493928 | A | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-1830A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493928 | ||||||
chr7:95493981 | T | A | 2 | a0001c0001t0001g0203a0001c0001t0002g0204 | 2 | HG02132.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.188-1777T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95493981 | ||||||
chr7:95494028 | T | A | 1 | a0001c0001t0016g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-1730T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494028 | ||||||
chr7:95494158 | A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.188-1600A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494158 | ||||||
chr7:95494161 | T | G | 3 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0015g0318 | 3 | HG01884.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188-1597T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494161 | ||||||
chr7:95494287 | A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(52): Show | 57 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.188-1471A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494287 | ||||||
chr7:95494598 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.188-1160T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494598 | ||||||
chr7:95494677 | T | A | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-1081T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494677 | ||||||
chr7:95494701 | G | C | 1 | a0001c0001t0003g0054 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.188-1057G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494701 | ||||||
chr7:95494876 | A | C | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-882A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95494876 | ||||||
chr7:95495017 | G | A | 1 | a0001c0001t0001g0336 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.188-741G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495017 | ||||||
chr7:95495069 | T | C | 128 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.188-689T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495069 | ||||||
chr7:95495098 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188-660T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495098 | ||||||
chr7:95495174 | C | A | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-584C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495174 | ||||||
chr7:95495174 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.188-584C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495174 | ||||||
chr7:95495187 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-571C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495187 | ||||||
chr7:95495207 | G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(98): Show | 105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.188-551G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495207 | ||||||
chr7:95495242 | T | A | 1 | a0002c0002t0003g0371 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.188-516T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495242 | ||||||
chr7:95495380 | T | A | 1 | a0001c0001t0003g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.188-378T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495380 | ||||||
chr7:95495539 | C | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-219C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495539 | ||||||
chr7:95495591 | C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(70): Show | 75 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.188-167C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495591 | ||||||
chr7:95495643 | C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.188-115C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495643 | ||||||
chr7:95495658 | T | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0177 | 2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.188-100T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | chr7 | 95495658 | ||||||
chr7:95495738 | C | CT | 32 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0049others(29): Show | 32 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.188-4dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | |||||
chr7:95495738 | CT | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(36): Show | 39 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.188-4delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | |||||
chr7:95495738 | CTT | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
splice_region_variant&intron_variant | LOW | c.188-5_188-4delTT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 95495738 | |||||
chr7:95496150 | A | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+93A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496150 | ||||||
chr7:95496388 | G | A | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+331G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496388 | ||||||
chr7:95496420 | A | G | 1 | a0001c0001t0003g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.487+363A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496420 | ||||||
chr7:95496477 | A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(77): Show | 84 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.487+420A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496477 | ||||||
chr7:95496515 | C | A | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+458C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496515 | ||||||
chr7:95496619 | A | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+562A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496619 | ||||||
chr7:95496631 | G | A | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+574G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496631 | ||||||
chr7:95496644 | C | T | 3 | a0002c0002t0004g0037a0002c0002t0006g0036a0002c0002t0006g0038 | 3 | HG02451.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.487+587C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496644 | ||||||
chr7:95496697 | A | C | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+640A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496697 | ||||||
chr7:95496705 | G | A | 2 | a0001c0001t0009g0250a0001c0001t0009g0302 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.487+648G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496705 | ||||||
chr7:95496864 | A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(52): Show | 57 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.487+807A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95496864 | ||||||
chr7:95497031 | G | A | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+974G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497031 | ||||||
chr7:95497072 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.487+1015G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497072 | ||||||
chr7:95497094 | G | A | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+1037G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497094 | ||||||
chr7:95497111 | GC | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1056delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95497111 | |||||
chr7:95497209 | T | C | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092 | 3 | HG01256.hp1 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.487+1152T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497209 | ||||||
chr7:95497401 | T | G | 1 | a0001c0001t0004g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.487+1344T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497401 | ||||||
chr7:95497492 | G | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+1435G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497492 | ||||||
chr7:95497523 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+1466T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497523 | ||||||
chr7:95497523 | T | G | 124 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(121): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+1466T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497523 | ||||||
chr7:95497625 | T | G | 7 | a0001c0001t0004g0022a0001c0001t0004g0084a0001c0001t0009g0019others(4): Show | 7 | HG02451.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1568T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497625 | ||||||
chr7:95497633 | T | C | 1 | a0001c0001t0010g0185 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.487+1576T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497633 | ||||||
chr7:95497658 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.487+1601A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497658 | ||||||
chr7:95497766 | A | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(111): Show | 118 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(115): Show |
intron_variant | MODIFIER | c.487+1709A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497766 | ||||||
chr7:95497899 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1842T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497899 | ||||||
chr7:95497922 | C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(111): Show | 118 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(115): Show |
intron_variant | MODIFIER | c.487+1865C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95497922 | ||||||
chr7:95498043 | G | T | 1 | a0001c0001t0001g0366 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.487+1986G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498043 | ||||||
chr7:95498199 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.487+2142G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498199 | ||||||
chr7:95498222 | G | C | 127 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(124): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+2165G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498222 | ||||||
chr7:95498342 | C | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+2285C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498342 | ||||||
chr7:95498385 | C | G | 2 | a0002c0002t0004g0028a0002c0002t0004g0029 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.487+2328C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498385 | ||||||
chr7:95498487 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+2430T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498487 | ||||||
chr7:95498606 | A | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(98): Show | 105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+2549A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498606 | ||||||
chr7:95498607 | T | C | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+2550T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498607 | ||||||
chr7:95498692 | G | A | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+2635G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498692 | ||||||
chr7:95498748 | A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0181others(60): Show | 65 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.487+2691A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498748 | ||||||
chr7:95498750 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+2693G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498750 | ||||||
chr7:95498864 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.487+2807G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498864 | ||||||
chr7:95498987 | A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02027.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.487+2930A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95498987 | ||||||
chr7:95499296 | A | G | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+3239A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499296 | ||||||
chr7:95499315 | A | G | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3258A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499315 | ||||||
chr7:95499337 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+3280T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499337 | ||||||
chr7:95499364 | G | T | 127 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(124): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+3307G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499364 | ||||||
chr7:95499384 | A | C | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3327A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499384 | ||||||
chr7:95499441 | G | A | 305 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.487+3384G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499441 | ||||||
chr7:95499710 | A | G | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0037others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+3653A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499710 | ||||||
chr7:95499766 | T | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 8 | HG00735.hp1 HG01358.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+3709T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499766 | ||||||
chr7:95499794 | C | T | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+3737C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499794 | ||||||
chr7:95499860 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.487+3803A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499860 | ||||||
chr7:95499865 | C | CT | 8 | a0001c0001t0001g0016a0001c0001t0001g0332a0001c0001t0001g0334others(5): Show | 8 | HG01175.hp1 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+3834dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | |||||
chr7:95499865 | CT | C | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.487+3834delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | |||||
chr7:95499865 | CTT | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0049others(69): Show | 73 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.487+3833_487+3834d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | |||||
chr7:95499865 | CTTT | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0181a0001c0001t0003g0094others(14): Show | 17 | HG01070.hp1 HG01192.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+3832_487+3834d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95499865 | |||||
chr7:95499912 | C | T | 1 | a0002c0002t0003g0371 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487+3855C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499912 | ||||||
chr7:95499913 | G | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+3856G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499913 | ||||||
chr7:95499942 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.487+3885C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499942 | ||||||
chr7:95499974 | C | T | 2 | a0001c0001t0003g0117a0002c0002t0006g0372 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.487+3917C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95499974 | ||||||
chr7:95500011 | G | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(121): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.487+3954G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500011 | ||||||
chr7:95500016 | C | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+3959C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500016 | ||||||
chr7:95500036 | C | G | 1 | a0001c0001t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.487+3979C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500036 | ||||||
chr7:95500039 | A | G | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+3982A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500039 | ||||||
chr7:95500103 | G | A | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+4046G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500103 | ||||||
chr7:95500209 | G | C | 1 | a0001c0001t0004g0319 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.487+4152G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500209 | ||||||
chr7:95500270 | A | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA19002.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.487+4213A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500270 | ||||||
chr7:95500294 | C | T | 1 | a0005c0003t0016g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.487+4237C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500294 | ||||||
chr7:95500295 | G | A | 10 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+4238G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500295 | ||||||
chr7:95500471 | C | G | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+4414C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500471 | ||||||
chr7:95500492 | C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+4435C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500492 | ||||||
chr7:95500522 | A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.487+4465A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500522 | ||||||
chr7:95500568 | C | CA | 50 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0064others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.487+4539dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | C | CAA | 10 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(7): Show | 10 | HG01255.hp2 HG02647.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+4538_487+4539d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | CA | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0116others(77): Show | 84 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.487+4539delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | CAA | C | 19 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0174others(16): Show | 19 | HG00609.hp2 HG00639.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.487+4538_487+4539d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | CAAA | C | 19 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0332others(16): Show | 19 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.487+4537_487+4539d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | CAAAA | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(35): Show | 40 | HG00280.hp2 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.487+4536_487+4539d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500568 | CAAAAAA | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0115others(4): Show | 7 | HG01192.hp1 HG01433.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+4534_487+4539d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95500568 | |||||
chr7:95500832 | A | G | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG02615.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+4775A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95500832 | ||||||
chr7:95501125 | C | G | 1 | a0001c0001t0002g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487+5068C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501125 | ||||||
chr7:95501301 | G | T | 1 | a0001c0001t0003g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+5244G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501301 | ||||||
chr7:95501329 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.487+5272C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501329 | ||||||
chr7:95501332 | C | T | 5 | a0001c0001t0003g0052a0001c0001t0004g0023a0001c0001t0005g0024others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5275C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501332 | ||||||
chr7:95501460 | G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(98): Show | 105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+5403G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501460 | ||||||
chr7:95501512 | G | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5455G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501512 | ||||||
chr7:95501564 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.487+5507T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501564 | ||||||
chr7:95501646 | A | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+5589A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501646 | ||||||
chr7:95501700 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+5643T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501700 | ||||||
chr7:95501724 | T | G | 1 | a0001c0001t0025g0268 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.487+5667T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501724 | ||||||
chr7:95501866 | T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0343a0001c0001t0001g0349others(4): Show | 8 | HG00597.hp2 HG02027.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+5809T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501866 | ||||||
chr7:95501905 | C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.487+5848C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501905 | ||||||
chr7:95501932 | G | A | 8 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+5875G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501932 | ||||||
chr7:95501998 | C | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.487+5941C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95501998 | ||||||
chr7:95502014 | C | G | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+5957C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502014 | ||||||
chr7:95502068 | C | A | 1 | a0001c0001t0003g0067 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.487+6011C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502068 | ||||||
chr7:95502069 | G | A | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+6012G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502069 | ||||||
chr7:95502106 | TA | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0048others(67): Show | 71 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.487+6059delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502106 | |||||
chr7:95502275 | C | A | 308 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.487+6218C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502275 | ||||||
chr7:95502276 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+6219T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502276 | ||||||
chr7:95502339 | T | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.487+6282T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502339 | ||||||
chr7:95502386 | G | GC | 3 | a0001c0001t0001g0137a0001c0001t0001g0158a0001c0001t0001g0315 | 3 | HG01261.hp2 HG02056.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.487+6331dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502386 | |||||
chr7:95502389 | T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(74): Show | 81 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+6332T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502389 | ||||||
chr7:95502389 | T | TG | 6 | a0001c0001t0001g0016a0001c0001t0004g0013a0001c0001t0010g0182others(3): Show | 6 | HG01192.hp1 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+6333dupG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502389 | |||||
chr7:95502389 | TGC | T | 131 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0194others(128): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.487+6334_487+6335d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502389 | |||||
chr7:95502390 | G | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0120others(74): Show | 81 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+6333G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502390 | ||||||
chr7:95502390 | GC | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0048others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.487+6334delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502390 | ||||||
chr7:95502391 | C | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(98): Show | 105 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+6334C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502391 | ||||||
chr7:95502391 | CG | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(48): Show | 53 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.487+6344delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95502391 | |||||
chr7:95502399 | G | C | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+6342G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502399 | ||||||
chr7:95502400 | G | C | 1 | a0001c0001t0015g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.487+6343G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502400 | ||||||
chr7:95502493 | A | G | 6 | a0001c0001t0002g0300a0001c0001t0003g0052a0001c0001t0004g0023others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+6436A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502493 | ||||||
chr7:95502655 | A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(97): Show | 104 | HG00423.hp1 HG00609.hp2 HG01099.hp2 others(101): Show |
intron_variant | MODIFIER | c.487+6598A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95502655 | ||||||
chr7:95503044 | G | A | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487+6987G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503044 | ||||||
chr7:95503064 | A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA19002.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.487+7007A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503064 | ||||||
chr7:95503085 | A | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0321others(45): Show | 50 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.487+7028A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503085 | ||||||
chr7:95503091 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+7034A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503091 | ||||||
chr7:95503212 | G | A | 1 | a0002c0002t0006g0372 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.487+7155G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503212 | ||||||
chr7:95503717 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.487+7660A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503717 | ||||||
chr7:95503741 | C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02647.hp2 HG02698.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+7684C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503741 | ||||||
chr7:95503938 | T | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(54): Show | 59 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.487+7881T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95503938 | ||||||
chr7:95504131 | T | C | 26 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(23): Show | 26 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.487+8074T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504131 | ||||||
chr7:95504135 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.487+8078A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504135 | ||||||
chr7:95504350 | A | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 31 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+8293A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504350 | ||||||
chr7:95504354 | CAT | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 31 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+8298_487+8299d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504354 | ||||||
chr7:95504437 | T | G | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+8380T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504437 | ||||||
chr7:95504478 | C | G | 2 | a0001c0001t0002g0118a0001c0001t0002g0177 | 2 | NA19059.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.487+8421C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504478 | ||||||
chr7:95504704 | C | T | 177 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(174): Show | 182 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.487+8647C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504704 | ||||||
chr7:95504931 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.487+8874C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504931 | ||||||
chr7:95504947 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.487+8890C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95504947 | ||||||
chr7:95505073 | G | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.487+9016G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505073 | ||||||
chr7:95505295 | TTGCATTT others(11): Show |
T | 2 | a0002c0002t0004g0028a0002c0002t0004g0029 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.487+9239_487+9256d others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505295 | ||||||
chr7:95505406 | G | A | 4 | a0001c0001t0001g0087a0001c0001t0004g0085a0001c0001t0004g0086others(1): Show | 4 | HG00735.hp2 HG01346.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9349G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505406 | ||||||
chr7:95505683 | G | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.487+9626G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505683 | ||||||
chr7:95505686 | T | TC | 15 | a0001c0001t0001g0359a0001c0001t0002g0134a0001c0001t0002g0135others(12): Show | 15 | HG01175.hp1 HG02055.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+9641dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95505686 | |||||
chr7:95505686 | TC | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(188): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.487+9641delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95505686 | |||||
chr7:95505692 | C | G | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+9635C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505692 | ||||||
chr7:95505694 | C | A | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+9637C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505694 | ||||||
chr7:95505696 | C | A | 3 | a0001c0001t0004g0338a0001c0001t0004g0341a0001c0001t0011g0041 | 3 | HG01243.hp2 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.487+9639C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | ||||||
chr7:95505696 | C | CG | 5 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+9639_487+9640i others(3): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | ||||||
chr7:95505696 | C | G | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+9639C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505696 | ||||||
chr7:95505697 | C | A | 26 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(23): Show | 26 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+9640C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505697 | ||||||
chr7:95505697 | C | T | 4 | a0001c0001t0005g0285a0001c0001t0005g0289a0001c0001t0005g0294others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9640C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505697 | ||||||
chr7:95505848 | C | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0138 | 2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.487+9791C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505848 | ||||||
chr7:95505961 | A | G | 3 | a0001c0001t0004g0129a0001c0001t0004g0146a0001c0001t0004g0161 | 3 | NA18945.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.487+9904A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505961 | ||||||
chr7:95505967 | C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0156 | 4 | HG02738.hp1 HG03239.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+9910C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95505967 | ||||||
chr7:95506049 | T | TGCCTGGC others(319): Show |
1 | a0001c0001t0001g0272 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.487+10007_487+1000 others(330): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506049 | |||||
chr7:95506051 | C | A | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+9994C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506051 | ||||||
chr7:95506152 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.487+10095G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506152 | ||||||
chr7:95506243 | A | G | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+10186A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506243 | ||||||
chr7:95506302 | T | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(169): Show | 177 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.487+10245T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506302 | ||||||
chr7:95506305 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.487+10248G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506305 | ||||||
chr7:95506521 | C | T | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+10464C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506521 | ||||||
chr7:95506657 | T | A | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(169): Show | 177 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.487+10600T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506657 | ||||||
chr7:95506686 | C | CT | 20 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0145others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.487+10647dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506686 | |||||
chr7:95506686 | CT | C | 158 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(155): Show | 163 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.487+10647delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95506686 | |||||
chr7:95506742 | T | G | 2 | a0001c0001t0004g0100a0001c0001t0004g0107 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.487+10685T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506742 | ||||||
chr7:95506825 | T | G | 14 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0023others(11): Show | 14 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+10768T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95506825 | ||||||
chr7:95507018 | C | G | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+10961C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507018 | ||||||
chr7:95507105 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+11048T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507105 | ||||||
chr7:95507150 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.487+11093G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507150 | ||||||
chr7:95507154 | T | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(85): Show | 90 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.487+11097T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507154 | ||||||
chr7:95507249 | C | T | 17 | a0001c0001t0002g0204a0001c0001t0003g0376a0001c0001t0003g0377others(14): Show | 17 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+11192C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507249 | ||||||
chr7:95507250 | G | A | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.487+11193G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507250 | ||||||
chr7:95507279 | G | A | 1 | a0001c0001t0005g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.487+11222G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507279 | ||||||
chr7:95507407 | G | C | 1 | a0001c0001t0003g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+11350G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507407 | ||||||
chr7:95507424 | A | C | 1 | a0001c0001t0001g0373 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.487+11367A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507424 | ||||||
chr7:95507664 | T | G | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487+11607T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507664 | ||||||
chr7:95507669 | G | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0214a0001c0001t0001g0322others(13): Show | 17 | HG02165.hp2 NA18944.hp1 NA18947.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+11612G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507669 | ||||||
chr7:95507838 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+11781C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507838 | ||||||
chr7:95507913 | C | CAATGAGT others(4): Show |
1 | a0001c0001t0002g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.487+11857_487+1186 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95507913 | |||||
chr7:95507955 | T | C | 5 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+11898T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95507955 | ||||||
chr7:95508250 | T | C | 3 | a0001c0001t0002g0111a0001c0001t0003g0112a0001c0001t0015g0113 | 3 | HG03471.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.487+12193T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508250 | ||||||
chr7:95508452 | C | A | 1 | a0001c0001t0015g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487+12395C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508452 | ||||||
chr7:95508638 | G | C | 1 | a0001c0001t0016g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.487+12581G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508638 | ||||||
chr7:95508729 | A | T | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+12672A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508729 | ||||||
chr7:95508980 | A | T | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+12923A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95508980 | ||||||
chr7:95509365 | G | C | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.487+13308G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509365 | ||||||
chr7:95509443 | A | G | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(344): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.487+13386A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509443 | ||||||
chr7:95509690 | C | T | 8 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(5): Show | 8 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+13633C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509690 | ||||||
chr7:95509884 | T | C | 8 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(5): Show | 8 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+13827T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509884 | ||||||
chr7:95509903 | A | G | 1 | a0001c0001t0003g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.487+13846A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509903 | ||||||
chr7:95509933 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.487+13876C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95509933 | ||||||
chr7:95510066 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.487+14009A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510066 | ||||||
chr7:95510126 | T | TA | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.487+14079dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95510126 | |||||
chr7:95510579 | A | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0063others(63): Show | 68 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.487+14522A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510579 | ||||||
chr7:95510719 | C | T | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 31 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.487+14662C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510719 | ||||||
chr7:95510810 | C | T | 2 | a0001c0001t0016g0370a0005c0003t0016g0053 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.487+14753C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510810 | ||||||
chr7:95510857 | A | T | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+14800A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510857 | ||||||
chr7:95510858 | G | A | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(170): Show | 178 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.487+14801G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95510858 | ||||||
chr7:95511264 | A | T | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.487+15207A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511264 | ||||||
chr7:95511450 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.487+15393C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511450 | ||||||
chr7:95511558 | A | T | 1 | a0001c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.487+15501A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511558 | ||||||
chr7:95511603 | G | A | 6 | a0001c0001t0002g0300a0001c0001t0005g0286a0001c0001t0005g0340others(3): Show | 6 | HG00741.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+15546G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511603 | ||||||
chr7:95511662 | C | CA | 25 | a0001c0001t0001g0051a0001c0001t0001g0170a0001c0001t0001g0181others(22): Show | 25 | HG00639.hp1 HG01192.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.487+15617dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95511662 | |||||
chr7:95511670 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.487+15613A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511670 | ||||||
chr7:95511671 | A | T | 8 | a0001c0001t0001g0331a0001c0001t0002g0004a0001c0001t0002g0135others(5): Show | 9 | HG01496.hp1 HG01928.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+15614A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511671 | ||||||
chr7:95511675 | T | A | 1 | a0001c0001t0013g0196 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+15618T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511675 | ||||||
chr7:95511843 | G | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0148 | 3 | NA18974.hp1 NA18993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.487+15786G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511843 | ||||||
chr7:95511856 | A | G | 2 | a0001c0001t0016g0370a0005c0003t0016g0053 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.487+15799A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511856 | ||||||
chr7:95511881 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.487+15824G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511881 | ||||||
chr7:95511885 | C | T | 2 | a0001c0001t0004g0319a0001c0001t0004g0320 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.487+15828C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511885 | ||||||
chr7:95511906 | A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+15849A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511906 | ||||||
chr7:95511960 | GT | G | 5 | a0001c0001t0005g0286a0001c0001t0005g0340a0001c0001t0007g0287others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-15848delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95511960 | |||||
chr7:95511971 | A | C | 1 | a0001c0001t0001g0051 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.488-15842A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95511971 | ||||||
chr7:95512110 | T | TC | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-15701dupC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95512110 | |||||
chr7:95512247 | C | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(171): Show | 179 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.488-15566C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512247 | ||||||
chr7:95512396 | C | T | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-15417C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512396 | ||||||
chr7:95512424 | A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0116others(34): Show | 38 | HG00408.hp2 HG00609.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.488-15389A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512424 | ||||||
chr7:95512451 | G | A | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-15362G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512451 | ||||||
chr7:95512748 | G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02647.hp2 HG02698.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-15065G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512748 | ||||||
chr7:95512753 | A | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 37 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.488-15060A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512753 | ||||||
chr7:95512968 | G | A | 37 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 37 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.488-14845G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95512968 | ||||||
chr7:95513029 | G | A | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14784G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513029 | ||||||
chr7:95513075 | T | C | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-14738T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513075 | ||||||
chr7:95513081 | G | A | 5 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14732G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513081 | ||||||
chr7:95513101 | C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.488-14712C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513101 | ||||||
chr7:95513142 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.488-14671G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513142 | ||||||
chr7:95513233 | G | GT | 5 | a0001c0001t0001g0106a0001c0001t0001g0237a0001c0001t0001g0242others(2): Show | 5 | HG02602.hp2 HG03688.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-14572dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513233 | |||||
chr7:95513242 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.488-14571G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513242 | ||||||
chr7:95513252 | TG | T | 37 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(34): Show | 40 | HG00423.hp1 HG01496.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.488-14560delG | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513252 | ||||||
chr7:95513253 | G | GTT | 11 | a0001c0001t0006g0133a0001c0001t0006g0155a0002c0002t0004g0037others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-14540_488-1453 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | |||||
chr7:95513253 | G | T | 5 | a0001c0001t0002g0131a0001c0001t0002g0156a0001c0001t0002g0364others(2): Show | 5 | HG00738.hp2 HG02486.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-14560G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513253 | ||||||
chr7:95513253 | GT | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.488-14539delT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | |||||
chr7:95513253 | GTT | G | 66 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0087others(63): Show | 66 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.488-14540_488-1453 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | |||||
chr7:95513253 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-14550_488-1453 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513253 | |||||
chr7:95513256 | T | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0005g0285others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-14557T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513256 | ||||||
chr7:95513258 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.488-14555T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513258 | ||||||
chr7:95513260 | T | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0149 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.488-14553T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513260 | ||||||
chr7:95513293 | A | ATG | 9 | a0001c0001t0001g0062a0001c0001t0001g0209a0001c0001t0001g0229others(6): Show | 9 | HG01081.hp2 HG02109.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-14482_488-1448 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | A | ATGTG | 66 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0087others(63): Show | 66 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.488-14484_488-1448 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | A | ATGTGTG | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.488-14486_488-1448 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | A | ATGTGTGT others(1): Show |
39 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-14488_488-1448 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | A | ATGTGTGT others(3): Show |
32 | a0001c0001t0001g0215a0001c0001t0001g0247a0001c0001t0001g0263others(29): Show | 32 | HG00597.hp1 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.488-14490_488-1448 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0003g0045others(1): Show | 4 | HG00639.hp2 HG01106.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-14492_488-1448 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATG | A | 13 | a0001c0001t0001g0212a0001c0001t0001g0317a0001c0001t0002g0132others(10): Show | 13 | HG00423.hp1 HG01192.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.488-14482_488-1448 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATGTG | A | 41 | a0001c0001t0001g0063a0001c0001t0001g0205a0001c0001t0001g0269others(38): Show | 44 | HG00673.hp1 HG00738.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-14484_488-1448 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATGTGTG | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0214others(18): Show | 22 | HG01243.hp2 HG01256.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.488-14486_488-1448 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATGTGTGT others(1): Show |
A | 50 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0049others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-14488_488-1448 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATGTGTGT others(3): Show |
A | 9 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.488-14490_488-1448 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513293 | ATGTGTGT others(9): Show |
A | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-14496_488-1448 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95513293 | |||||
chr7:95513303 | G | C | 1 | a0001c0001t0016g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-14510G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513303 | ||||||
chr7:95513448 | G | A | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-14365G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513448 | ||||||
chr7:95513492 | G | A | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-14321G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513492 | ||||||
chr7:95513569 | G | T | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-14244G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513569 | ||||||
chr7:95513607 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488-14206C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513607 | ||||||
chr7:95513831 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.488-13982A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513831 | ||||||
chr7:95513859 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.488-13954G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513859 | ||||||
chr7:95513927 | C | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-13886C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513927 | ||||||
chr7:95513929 | C | T | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-13884C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95513929 | ||||||
chr7:95514021 | A | C | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-13792A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514021 | ||||||
chr7:95514030 | G | C | 1 | a0001c0001t0001g0348 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.488-13783G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514030 | ||||||
chr7:95514197 | A | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0332 | 2 | NA18949.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.488-13616A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514197 | ||||||
chr7:95514231 | G | C | 1 | a0005c0003t0016g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.488-13582G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514231 | ||||||
chr7:95514447 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.488-13366A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514447 | ||||||
chr7:95514631 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.488-13182G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514631 | ||||||
chr7:95514688 | G | T | 1 | a0001c0001t0001g0331 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.488-13125G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514688 | ||||||
chr7:95514830 | T | G | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-12983T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514830 | ||||||
chr7:95514937 | C | G | 1 | a0001c0001t0002g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.488-12876C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95514937 | ||||||
chr7:95515090 | G | T | 1 | a0001c0001t0004g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.488-12723G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515090 | ||||||
chr7:95515145 | TTTTC | T | 49 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0049others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-12654_488-1265 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515145 | |||||
chr7:95515155 | T | TTC | 8 | a0001c0001t0001g0343a0001c0001t0001g0350a0001c0001t0001g0353others(5): Show | 8 | HG00738.hp2 HG01516.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12656_488-1265 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515155 | |||||
chr7:95515155 | TTCTTTC | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0004c0004t0004g0105 | 3 | HG02698.hp2 HG03710.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.488-12644_488-1263 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515155 | |||||
chr7:95515157 | CTTTCTCT others(1): Show |
C | 10 | a0001c0001t0001g0180a0001c0001t0001g0324a0001c0001t0001g0329others(7): Show | 11 | HG01496.hp1 HG01952.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.488-12654_488-1264 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515157 | |||||
chr7:95515159 | T | C | 59 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0214others(56): Show | 61 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.488-12654T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515159 | ||||||
chr7:95515161 | C | CTCTCTT | 5 | a0001c0001t0001g0317a0001c0001t0001g0366a0001c0001t0002g0148others(2): Show | 5 | HG02572.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12649_488-1264 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | |||||
chr7:95515161 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.488-12652C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515161 | ||||||
chr7:95515161 | CTCTT | C | 9 | a0001c0001t0004g0088a0001c0001t0004g0100a0001c0001t0004g0101others(6): Show | 9 | HG01346.hp2 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-12648_488-1264 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | |||||
chr7:95515161 | CTCTTTCT others(3): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.488-12644_488-1263 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515161 | |||||
chr7:95515163 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.488-12650C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515163 | ||||||
chr7:95515163 | CTT | C | 3 | a0001c0001t0003g0376a0001c0001t0004g0099a0001c0001t0012g0378 | 3 | HG00621.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.488-12648_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515163 | CTTTCTCT others(1): Show |
C | 4 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0005g0026others(1): Show | 4 | HG00438.hp2 HG01192.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12648_488-1264 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515163 | CTTTCTCT others(5): Show |
C | 10 | a0001c0001t0001g0181a0001c0001t0001g0347a0001c0001t0002g0300others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12648_488-1263 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515163 | CTTTCTCT others(9): Show |
C | 4 | a0001c0001t0001g0358a0001c0001t0006g0155a0002c0002t0006g0035others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12648_488-1263 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515163 | CTTTCTCT others(21): Show |
C | 1 | a0001c0001t0002g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.488-12648_488-1262 others(32): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515163 | CTTTCTCT others(29): Show |
C | 2 | a0001c0001t0003g0309a0001c0001t0011g0021 | 2 | HG01192.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.488-12648_488-1261 others(40): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515163 | |||||
chr7:95515165 | T | C | 110 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(107): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.488-12648T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515165 | ||||||
chr7:95515165 | TTC | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0152a0001c0001t0004g0011others(1): Show | 4 | HG02723.hp2 HG03704.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12644_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515165 | |||||
chr7:95515167 | C | CTCTCTTT others(7): Show |
1 | a0001c0001t0001g0243 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.488-12643_488-1264 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTCTT | 23 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0141others(20): Show | 23 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.488-12584_488-1258 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTCTTCTT others(4): Show |
1 | a0001c0001t0003g0377 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.488-12642_488-1264 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTCTTTCT others(1): Show |
16 | a0001c0001t0001g0040a0001c0001t0001g0062a0001c0001t0001g0142others(13): Show | 16 | HG00639.hp1 HG01261.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12588_488-1258 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTCTTTCT others(5): Show |
10 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0246others(7): Show | 10 | HG00639.hp2 HG01952.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12592_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTCTTTCT others(9): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0210a0001c0001t0001g0245 | 3 | HG00621.hp2 HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.488-12596_488-1258 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | CTT | 16 | a0001c0001t0001g0010a0001c0001t0001g0317a0001c0001t0001g0343others(13): Show | 16 | HG00738.hp2 HG01516.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12645_488-1264 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | C | T | 32 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0214others(29): Show | 34 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.488-12646C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515167 | ||||||
chr7:95515167 | CTCTT | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0116others(43): Show | 47 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.488-12584_488-1258 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | CTCTTTCT others(1): Show |
C | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0128others(10): Show | 13 | HG01346.hp1 HG02132.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.488-12588_488-1258 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | CTCTTTCT others(5): Show |
C | 5 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0159others(2): Show | 5 | HG01099.hp1 HG02257.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12592_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515167 | CTCTTTCT others(9): Show |
C | 4 | a0001c0001t0003g0308a0001c0001t0013g0195a0001c0001t0013g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12596_488-1258 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515167 | |||||
chr7:95515171 | T | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0180a0001c0001t0001g0324others(18): Show | 22 | HG01346.hp2 HG01433.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.488-12642T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515171 | ||||||
chr7:95515175 | T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0005g0026others(1): Show | 4 | HG00438.hp2 HG01192.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12638T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515175 | ||||||
chr7:95515179 | T | C | 5 | a0001c0001t0001g0181a0001c0001t0004g0086a0001c0001t0005g0193others(2): Show | 5 | HG00735.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12634T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515179 | ||||||
chr7:95515190 | TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0004g0319a0001c0001t0004g0320 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.488-12620_488-1260 others(23): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515190 | |||||
chr7:95515195 | TTC | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0084a0001c0001t0011g0020others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12616_488-1261 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515195 | |||||
chr7:95515203 | T | C | 2 | a0001c0001t0003g0309a0001c0001t0011g0021 | 2 | HG01192.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.488-12610T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515203 | ||||||
chr7:95515215 | TTC | T | 3 | a0001c0001t0003g0055a0001c0001t0015g0318a0002c0002t0003g0371 | 3 | HG01175.hp2 HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.488-12596_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515215 | |||||
chr7:95515215 | TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0003g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.488-12596_488-1258 others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515215 | |||||
chr7:95515217 | C | CTT | 5 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0229others(2): Show | 5 | HG01256.hp2 HG04115.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12594_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515217 | |||||
chr7:95515218 | T | C | 5 | a0001c0001t0004g0022a0001c0001t0004g0084a0001c0001t0011g0020others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12595T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515218 | ||||||
chr7:95515219 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0007g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | |||||
chr7:95515219 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0004g0257 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.488-12581_488-1258 others(26): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | |||||
chr7:95515219 | TTC | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0234others(3): Show | 6 | HG00408.hp1 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12592_488-1259 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515219 | |||||
chr7:95515222 | T | TTTCTTTC others(13): Show |
1 | a0001c0001t0007g0255 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515222 | |||||
chr7:95515223 | TTC | T | 3 | a0001c0001t0001g0275a0001c0001t0003g0094a0001c0001t0018g0288 | 3 | HG01070.hp1 HG02071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.488-12588_488-1258 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515223 | |||||
chr7:95515229 | C | T | 9 | a0001c0001t0001g0160a0001c0001t0002g0001a0001c0001t0002g0076others(6): Show | 11 | HG00609.hp2 HG01109.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.488-12584C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515229 | ||||||
chr7:95515229 | CTT | C | 15 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0234others(12): Show | 15 | HG00408.hp1 HG01070.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.488-12580_488-1257 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515229 | |||||
chr7:95515230 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0158 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(15): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515230 | |||||
chr7:95515231 | T | C | 13 | a0001c0001t0001g0160a0001c0001t0002g0001a0001c0001t0002g0043others(10): Show | 15 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-12582T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515231 | ||||||
chr7:95515231 | T | TTC | 10 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0225others(7): Show | 10 | HG00621.hp1 HG01256.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-12581_488-1258 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | |||||
chr7:95515231 | T | TTCTTTCT others(5): Show |
1 | a0001c0001t0009g0260 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488-12581_488-1258 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | |||||
chr7:95515231 | TTTTC | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0180others(32): Show | 36 | HG00323.hp2 HG00597.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.488-12565_488-1256 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | |||||
chr7:95515231 | TTTTCTTT others(39): Show |
T | 1 | a0001c0001t0011g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.488-12561_488-1251 others(50): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515231 | |||||
chr7:95515233 | T | C | 54 | a0001c0001t0001g0063a0001c0001t0001g0125a0001c0001t0001g0205others(51): Show | 54 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.488-12580T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515233 | ||||||
chr7:95515235 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0002g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.488-12576_488-1256 others(18): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515235 | |||||
chr7:95515235 | C | T | 50 | a0001c0001t0001g0063a0001c0001t0001g0125a0001c0001t0001g0205others(47): Show | 50 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.488-12578C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515235 | ||||||
chr7:95515236 | T | C | 7 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0229others(4): Show | 7 | HG01256.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-12577T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515236 | ||||||
chr7:95515237 | TTCTTTCT others(23): Show |
T | 1 | a0001c0001t0004g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.488-12561_488-1253 others(34): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515237 | |||||
chr7:95515240 | T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0002g0111others(1): Show | 4 | HG01175.hp2 NA18974.hp2 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12573T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515240 | ||||||
chr7:95515241 | TTC | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0047a0001c0001t0009g0296 | 3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12570_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515241 | |||||
chr7:95515241 | TTCTTTCT others(19): Show |
T | 2 | a0001c0001t0004g0022a0001c0001t0021g0018 | 2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.488-12561_488-1253 others(30): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515241 | |||||
chr7:95515243 | C | CTT | 1 | a0001c0001t0002g0001 | 3 | HG02738.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.488-12568_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515243 | |||||
chr7:95515244 | T | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0253others(5): Show | 8 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12569T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515244 | ||||||
chr7:95515248 | T | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(31): Show | 36 | HG00423.hp1 HG00609.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.488-12565T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515248 | ||||||
chr7:95515249 | TTCCTTCT others(11): Show |
T | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-12561_488-1254 others(22): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515249 | |||||
chr7:95515251 | CCT | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0229others(3): Show | 6 | HG01256.hp2 HG01884.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12561_488-1256 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515251 | ||||||
chr7:95515252 | C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(60): Show | 67 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.488-12561C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515252 | ||||||
chr7:95515255 | CTT | C | 3 | a0001c0001t0001g0234a0001c0001t0002g0111a0001c0001t0003g0055 | 3 | HG01175.hp2 NA19091.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.488-12556_488-1255 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515255 | |||||
chr7:95515256 | T | C | 8 | a0001c0001t0001g0221a0001c0001t0001g0278a0001c0001t0003g0175others(5): Show | 8 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.488-12557T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515256 | ||||||
chr7:95515257 | T | TTC | 3 | a0001c0001t0002g0118a0001c0001t0002g0162a0002c0002t0004g0029 | 3 | HG02486.hp2 HG03017.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.488-12554_488-1255 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515257 | |||||
chr7:95515260 | T | C | 3 | a0001c0001t0002g0001a0001c0001t0004g0259a0001c0001t0005g0380 | 5 | HG02738.hp1 HG03239.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12553T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515260 | ||||||
chr7:95515261 | T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0253others(2): Show | 5 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12552T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515261 | ||||||
chr7:95515261 | T | TTC | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0321others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12550_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515261 | |||||
chr7:95515261 | TTCTTTC | T | 3 | a0001c0001t0001g0221a0001c0001t0003g0175a0001c0001t0007g0374 | 3 | NA18747.hp2 NA18995.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.488-12544_488-1253 others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515261 | |||||
chr7:95515263 | C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0253others(2): Show | 5 | HG00408.hp1 HG01243.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-12550C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515263 | ||||||
chr7:95515264 | T | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0047a0001c0001t0009g0296 | 3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12549T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515264 | ||||||
chr7:95515265 | T | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0160others(28): Show | 33 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.488-12548T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515265 | ||||||
chr7:95515265 | TTC | T | 14 | a0001c0001t0001g0209a0001c0001t0001g0229a0001c0001t0001g0234others(11): Show | 14 | HG01081.hp2 HG01175.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-12544_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515265 | |||||
chr7:95515267 | C | CTCTT | 13 | a0001c0001t0001g0214a0001c0001t0001g0345a0001c0001t0001g0366others(10): Show | 13 | HG00673.hp1 HG01099.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.488-12497_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0335a0001c0001t0008g0123a0001c0001t0008g0165 | 3 | HG01167.hp1 HG02602.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.488-12505_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | C | CTT | 16 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(13): Show | 18 | HG01243.hp2 HG01256.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12545_488-1254 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0160others(28): Show | 33 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.488-12546C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515267 | ||||||
chr7:95515267 | CTCTT | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0190others(35): Show | 39 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-12497_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | CTCTTTCT others(1): Show |
C | 16 | a0001c0001t0001g0180a0001c0001t0001g0194a0001c0001t0001g0347others(13): Show | 16 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.488-12501_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | CTCTTTCT others(5): Show |
C | 8 | a0001c0001t0001g0219a0001c0001t0002g0046a0001c0001t0002g0130others(5): Show | 8 | HG01891.hp2 HG03209.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-12505_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | CTCTTTCT others(9): Show |
C | 2 | a0001c0001t0002g0042a0001c0001t0002g0044 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.488-12509_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515267 | CTCTTTCT others(13): Show |
C | 3 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0001t0001g0362 | 3 | NA18975.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.488-12513_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515267 | |||||
chr7:95515268 | T | C | 2 | a0001c0001t0009g0019a0001c0001t0009g0250 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.488-12545T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515268 | ||||||
chr7:95515269 | C | T | 6 | a0001c0001t0001g0278a0001c0001t0005g0380a0001c0001t0007g0287others(3): Show | 6 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-12544C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515269 | ||||||
chr7:95515271 | T | C | 6 | a0001c0001t0001g0278a0001c0001t0005g0380a0001c0001t0007g0287others(3): Show | 6 | HG01169.hp1 HG01358.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-12542T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515271 | ||||||
chr7:95515273 | C | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-12540C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515273 | ||||||
chr7:95515275 | T | C | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-12538T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515275 | ||||||
chr7:95515277 | CTT | C | 3 | a0001c0001t0001g0221a0001c0001t0003g0175a0001c0001t0004g0259 | 3 | HG03486.hp2 NA18747.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.488-12534_488-1253 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515277 | |||||
chr7:95515279 | T | C | 1 | a0001c0001t0011g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.488-12534T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515279 | ||||||
chr7:95515281 | CTT | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0047a0001c0001t0009g0296 | 3 | HG01081.hp2 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.488-12530_488-1252 others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515281 | |||||
chr7:95515304 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.488-12509T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515304 | ||||||
chr7:95515304 | TCTTTCTT others(13): Show |
T | 1 | a0001c0001t0009g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.488-12505_488-1248 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515304 | |||||
chr7:95515308 | T | C | 18 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0209others(15): Show | 18 | HG00408.hp1 HG00438.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.488-12505T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515308 | ||||||
chr7:95515308 | TCTTTCTT others(5): Show |
T | 1 | a0001c0001t0016g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-12501_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515308 | |||||
chr7:95515312 | T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.488-12501T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515312 | ||||||
chr7:95515312 | T | TCTTC | 3 | a0001c0001t0001g0124a0001c0001t0001g0248a0001c0001t0002g0300 | 3 | HG00741.hp2 HG02735.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.488-12498_488-1249 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515312 | |||||
chr7:95515312 | T | TCTTCCTT others(1): Show |
4 | a0001c0001t0001g0220a0001c0001t0001g0242a0001c0001t0004g0161others(1): Show | 4 | HG00280.hp1 NA18966.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-12498_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515312 | |||||
chr7:95515316 | T | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(111): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.488-12497T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515316 | ||||||
chr7:95515316 | T | TCTTC | 50 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0027others(47): Show | 51 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-12481_488-1247 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTCCTT others(1): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0143a0001c0001t0002g0147others(1): Show | 5 | HG02165.hp1 HG03540.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-12485_488-1247 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTCCTT others(5): Show |
12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0212others(9): Show | 12 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.488-12489_488-1247 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTCCTT others(9): Show |
3 | a0001c0001t0001g0137a0001c0001t0001g0232a0001c0001t0001g0237 | 3 | HG02056.hp1 HG02056.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.488-12493_488-1247 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(1): Show |
32 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0120others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(12): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(5): Show |
1 | a0001c0001t0001g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488-12494_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(9): Show |
7 | a0001c0001t0001g0040a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG00438.hp1 HG00558.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(5): Show |
12 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0213others(9): Show | 12 | HG01070.hp2 HG01361.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.488-12494_488-1249 others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(13): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0231 | 2 | HG02015.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.488-12494_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(9): Show |
3 | a0001c0001t0001g0164a0001c0001t0002g0134a0001c0001t0003g0072 | 3 | NA19002.hp2 NA19009.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.488-12494_488-1249 others(20): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515316 | T | TCTTTCTT others(13): Show |
1 | a0001c0001t0002g0151 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.488-12494_488-1249 others(24): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515316 | |||||
chr7:95515320 | C | T | 1 | a0001c0001t0009g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.488-12493C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515320 | ||||||
chr7:95515324 | C | T | 1 | a0001c0001t0009g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.488-12489C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515324 | ||||||
chr7:95515328 | C | T | 1 | a0001c0001t0021g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488-12485C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515328 | ||||||
chr7:95515332 | C | T | 4 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0011g0041others(1): Show | 4 | HG01192.hp2 HG02451.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-12481C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515332 | ||||||
chr7:95515336 | T | C | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(77): Show | 83 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.488-12477T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515336 | ||||||
chr7:95515340 | T | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0317a0001c0001t0002g0001others(38): Show | 44 | HG00423.hp1 HG00738.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-12473T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515340 | ||||||
chr7:95515350 | TTTTTCTT others(6): Show |
T | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-12441_488-1242 others(17): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515350 | |||||
chr7:95515353 | T | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0087a0001c0001t0002g0300others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12460T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515353 | ||||||
chr7:95515355 | C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0087a0001c0001t0002g0300others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12458C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515355 | ||||||
chr7:95515364 | TTTTC | T | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0097others(20): Show | 23 | HG00438.hp2 HG01106.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.488-12437_488-1243 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515364 | |||||
chr7:95515367 | T | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0087a0001c0001t0002g0300others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12446T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515367 | ||||||
chr7:95515368 | C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0087a0001c0001t0002g0300others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12445C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515368 | ||||||
chr7:95515370 | T | C | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.488-12443T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515370 | ||||||
chr7:95515386 | C | CT | 14 | a0001c0001t0001g0075a0001c0001t0001g0178a0001c0001t0001g0198others(11): Show | 14 | HG00140.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-12419dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515386 | |||||
chr7:95515407 | T | C | 1 | a0001c0001t0003g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.488-12406T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515407 | ||||||
chr7:95515414 | TTCTC | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-12391_488-1238 others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515414 | |||||
chr7:95515424 | C | CT | 114 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(111): Show | 119 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.488-12379dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95515424 | |||||
chr7:95515425 | T | TC | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-12388_488-1238 others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515425 | ||||||
chr7:95515509 | G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 15 | HG00741.hp2 HG01192.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-12304G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515509 | ||||||
chr7:95515605 | G | A | 1 | a0001c0001t0014g0098 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.488-12208G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515605 | ||||||
chr7:95515827 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.488-11986C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515827 | ||||||
chr7:95515982 | C | A | 1 | a0001c0001t0002g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.488-11831C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95515982 | ||||||
chr7:95516116 | G | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-11697G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516116 | ||||||
chr7:95516306 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.488-11507T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516306 | ||||||
chr7:95516357 | A | G | 5 | a0001c0001t0005g0286a0001c0001t0005g0340a0001c0001t0007g0287others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-11456A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516357 | ||||||
chr7:95516495 | G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-11318G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516495 | ||||||
chr7:95516548 | T | C | 1 | a0001c0001t0003g0376 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.488-11265T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516548 | ||||||
chr7:95516595 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.488-11218G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516595 | ||||||
chr7:95516695 | T | C | 18 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-11118T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95516695 | ||||||
chr7:95517077 | G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 5 | HG00735.hp1 HG01358.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.488-10736G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517077 | ||||||
chr7:95517141 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.488-10672T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517141 | ||||||
chr7:95517143 | T | C | 3 | a0002c0002t0004g0037a0002c0002t0006g0036a0002c0002t0006g0038 | 3 | HG02451.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.488-10670T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517143 | ||||||
chr7:95517147 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.488-10666T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517147 | ||||||
chr7:95517215 | C | A | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-10598C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517215 | ||||||
chr7:95517313 | C | T | 41 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(38): Show | 44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-10500C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517313 | ||||||
chr7:95517369 | G | A | 18 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.488-10444G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517369 | ||||||
chr7:95517446 | T | G | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 43 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.488-10367T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517446 | ||||||
chr7:95517601 | G | GA | 30 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0023others(27): Show | 30 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.488-10201dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95517601 | |||||
chr7:95517614 | A | G | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-10199A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517614 | ||||||
chr7:95517782 | G | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0134a0001c0001t0002g0135others(8): Show | 12 | HG00423.hp1 HG01496.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.488-10031G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517782 | ||||||
chr7:95517800 | G | A | 1 | a0001c0001t0010g0187 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.488-10013G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517800 | ||||||
chr7:95517842 | G | A | 2 | a0001c0001t0011g0020a0001c0001t0011g0021 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.488-9971G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95517842 | ||||||
chr7:95518041 | G | A | 1 | a0001c0001t0015g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.488-9772G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518041 | ||||||
chr7:95518064 | G | A | 7 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0076others(4): Show | 7 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-9749G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518064 | ||||||
chr7:95518682 | A | T | 11 | a0001c0001t0006g0133a0001c0001t0006g0155a0002c0002t0004g0037others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-9131A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518682 | ||||||
chr7:95518736 | C | T | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-9077C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518736 | ||||||
chr7:95518762 | C | T | 1 | a0001c0001t0005g0340 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488-9051C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518762 | ||||||
chr7:95518852 | GAGATAAA others(5): Show |
G | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG00609.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.488-8960_488-8949d others(14): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518852 | ||||||
chr7:95518922 | A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-8891A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95518922 | ||||||
chr7:95519229 | T | C | 2 | a0001c0001t0004g0011a0001c0001t0004g0013 | 2 | HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.488-8584T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519229 | ||||||
chr7:95519653 | C | T | 5 | a0001c0001t0004g0022a0001c0001t0004g0084a0001c0001t0011g0020others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-8160C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519653 | ||||||
chr7:95519703 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.488-8110T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519703 | ||||||
chr7:95519748 | T | C | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-8065T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519748 | ||||||
chr7:95519792 | T | C | 11 | a0001c0001t0006g0133a0001c0001t0006g0155a0002c0002t0004g0037others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.488-8021T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95519792 | ||||||
chr7:95520163 | G | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(72): Show | 77 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.488-7650G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520163 | ||||||
chr7:95520362 | A | G | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-7451A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520362 | ||||||
chr7:95520482 | A | G | 5 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0004g0375others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-7331A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520482 | ||||||
chr7:95520642 | AC | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-7165delC | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95520642 | |||||
chr7:95520776 | T | C | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-7037T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520776 | ||||||
chr7:95520881 | G | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-6932G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520881 | ||||||
chr7:95520891 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.488-6922C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520891 | ||||||
chr7:95520919 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.488-6894T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95520919 | ||||||
chr7:95521064 | A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(73): Show | 78 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.488-6749A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521064 | ||||||
chr7:95521145 | A | C | 41 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(38): Show | 44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-6668A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521145 | ||||||
chr7:95521152 | T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-6661T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521152 | ||||||
chr7:95521274 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.488-6539A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521274 | ||||||
chr7:95521493 | T | C | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.488-6320T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521493 | ||||||
chr7:95521501 | A | G | 4 | a0001c0001t0003g0014a0001c0001t0003g0090a0001c0001t0003g0091others(1): Show | 4 | HG01255.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-6312A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521501 | ||||||
chr7:95521686 | T | TA | 49 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0103others(46): Show | 51 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.488-6114dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | |||||
chr7:95521686 | TA | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.488-6114delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | |||||
chr7:95521686 | TAA | T | 8 | a0001c0001t0001g0199a0001c0001t0001g0275a0001c0001t0003g0121others(5): Show | 8 | HG01099.hp2 HG01167.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.488-6115_488-6114d others(4): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521686 | |||||
chr7:95521796 | A | AT | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-6011dupT | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95521796 | |||||
chr7:95521818 | T | C | 10 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-5995T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521818 | ||||||
chr7:95521857 | A | C | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-5956A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521857 | ||||||
chr7:95521899 | A | G | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-5914A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521899 | ||||||
chr7:95521979 | T | C | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0076 | 3 | HG02257.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.488-5834T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95521979 | ||||||
chr7:95522064 | T | C | 2 | a0001c0001t0016g0370a0005c0003t0016g0053 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-5749T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522064 | ||||||
chr7:95522275 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.488-5538T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522275 | ||||||
chr7:95522314 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.488-5499G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522314 | ||||||
chr7:95522321 | G | A | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-5492G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522321 | ||||||
chr7:95522326 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.488-5487G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522326 | ||||||
chr7:95522345 | A | G | 10 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-5468A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522345 | ||||||
chr7:95522400 | AAAT | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(72): Show | 77 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.488-5408_488-5406d others(5): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95522400 | |||||
chr7:95522611 | G | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-5202G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522611 | ||||||
chr7:95522625 | T | C | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-5188T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522625 | ||||||
chr7:95522627 | T | C | 38 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0216others(35): Show | 38 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.488-5186T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522627 | ||||||
chr7:95522638 | C | G | 1 | a0001c0001t0009g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.488-5175C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522638 | ||||||
chr7:95522885 | T | C | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-4928T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95522885 | ||||||
chr7:95523068 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.488-4745A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523068 | ||||||
chr7:95523631 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.488-4182T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523631 | ||||||
chr7:95523725 | T | A | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-4088T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523725 | ||||||
chr7:95523748 | A | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02698.hp2 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.488-4065A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523748 | ||||||
chr7:95523866 | A | G | 1 | a0001c0001t0003g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.488-3947A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523866 | ||||||
chr7:95523870 | T | C | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3943T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523870 | ||||||
chr7:95523947 | C | T | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-3866C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523947 | ||||||
chr7:95523959 | G | C | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(172): Show | 180 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.488-3854G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523959 | ||||||
chr7:95523983 | G | A | 2 | a0001c0001t0016g0370a0005c0003t0016g0053 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-3830G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95523983 | ||||||
chr7:95524006 | A | G | 5 | a0001c0001t0002g0118a0001c0001t0002g0132a0001c0001t0002g0136others(2): Show | 5 | NA18974.hp1 NA18993.hp1 NA19059.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-3807A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524006 | ||||||
chr7:95524015 | A | G | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3798A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524015 | ||||||
chr7:95524062 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.488-3751C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524062 | ||||||
chr7:95524137 | G | A | 1 | a0001c0001t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488-3676G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524137 | ||||||
chr7:95524150 | T | C | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(170): Show | 178 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.488-3663T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524150 | ||||||
chr7:95524168 | A | G | 1 | a0003c0005t0001g0354 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.488-3645A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524168 | ||||||
chr7:95524240 | A | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.488-3573A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524240 | ||||||
chr7:95524327 | A | G | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-3486A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524327 | ||||||
chr7:95524373 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488-3440A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524373 | ||||||
chr7:95524498 | TA | T | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(169): Show | 177 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.488-3307delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95524498 | |||||
chr7:95524513 | A | G | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-3300A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524513 | ||||||
chr7:95524537 | C | G | 1 | a0001c0001t0003g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.488-3276C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524537 | ||||||
chr7:95524551 | T | C | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-3262T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524551 | ||||||
chr7:95524562 | T | C | 5 | a0001c0001t0004g0022a0001c0001t0004g0084a0001c0001t0011g0020others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-3251T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524562 | ||||||
chr7:95524697 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.488-3116G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524697 | ||||||
chr7:95524843 | G | T | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.488-2970G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524843 | ||||||
chr7:95524906 | C | T | 6 | a0001c0001t0001g0181a0001c0001t0010g0182a0001c0001t0010g0185others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-2907C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95524906 | ||||||
chr7:95525015 | C | T | 41 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(38): Show | 44 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.488-2798C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525015 | ||||||
chr7:95525139 | T | G | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 43 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.488-2674T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525139 | ||||||
chr7:95525217 | C | T | 1 | a0001c0001t0016g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.488-2596C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525217 | ||||||
chr7:95525218 | A | G | 39 | a0001c0001t0001g0317a0001c0001t0002g0001a0001c0001t0002g0004others(36): Show | 42 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.488-2595A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525218 | ||||||
chr7:95525369 | G | A | 1 | a0001c0001t0005g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.488-2444G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525369 | ||||||
chr7:95525370 | T | C | 3 | a0001c0001t0004g0110a0001c0001t0004g0259a0001c0001t0004g0261 | 3 | HG01891.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.488-2443T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525370 | ||||||
chr7:95525383 | T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.488-2430T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525383 | ||||||
chr7:95525474 | G | A | 1 | a0001c0001t0021g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488-2339G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525474 | ||||||
chr7:95525515 | A | C | 1 | a0002c0002t0012g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.488-2298A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525515 | ||||||
chr7:95525649 | C | G | 10 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-2164C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525649 | ||||||
chr7:95525733 | A | G | 1 | a0001c0001t0002g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.488-2080A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525733 | ||||||
chr7:95525812 | A | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(144): Show | 152 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.488-2001A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525812 | ||||||
chr7:95525882 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.488-1931A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525882 | ||||||
chr7:95525894 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.488-1919G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525894 | ||||||
chr7:95525944 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.488-1869G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95525944 | ||||||
chr7:95526025 | C | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-1788C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526025 | ||||||
chr7:95526026 | G | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0116others(35): Show | 39 | HG00408.hp2 HG00609.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.488-1787G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526026 | ||||||
chr7:95526154 | T | A | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-1659T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526154 | ||||||
chr7:95526218 | C | T | 10 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-1595C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526218 | ||||||
chr7:95526385 | G | C | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(376): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.488-1428G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526385 | ||||||
chr7:95526447 | C | T | 2 | a0001c0001t0016g0370a0005c0003t0016g0053 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.488-1366C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526447 | ||||||
chr7:95526454 | TCATA | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 56 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.488-1353_488-1350d others(6): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 95526454 | |||||
chr7:95526466 | T | G | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(114): Show | 122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.488-1347T>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526466 | ||||||
chr7:95526598 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.488-1215G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526598 | ||||||
chr7:95526950 | C | A | 4 | a0001c0001t0005g0285a0001c0001t0005g0289a0001c0001t0005g0294others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-863C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95526950 | ||||||
chr7:95527022 | T | A | 4 | a0001c0001t0005g0285a0001c0001t0005g0289a0001c0001t0005g0294others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-791T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527022 | ||||||
chr7:95527064 | T | A | 2 | a0001c0001t0004g0022a0001c0001t0004g0084 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.488-749T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527064 | ||||||
chr7:95527099 | A | G | 379 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(376): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.488-714A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527099 | ||||||
chr7:95527111 | T | C | 6 | a0001c0001t0003g0309a0001c0001t0004g0022a0001c0001t0004g0084others(3): Show | 6 | HG01192.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-702T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527111 | ||||||
chr7:95527233 | G | C | 9 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.488-580G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527233 | ||||||
chr7:95527433 | C | T | 10 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.488-380C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527433 | ||||||
chr7:95527472 | T | C | 5 | a0001c0001t0004g0023a0001c0001t0005g0024a0001c0001t0005g0025others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-341T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527472 | ||||||
chr7:95527557 | C | CT | 6 | a0001c0001t0007g0374a0001c0001t0009g0019a0001c0001t0009g0250others(3): Show | 6 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-256_488-255ins others(1): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 2/4 | chr7 | 95527557 | ||||||
chr7:95528353 | C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0136a0001c0001t0002g0148 | 3 | NA18974.hp1 NA18993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.978+50C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528353 | ||||||
chr7:95528406 | C | T | 7 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0005g0024others(4): Show | 7 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+103C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528406 | ||||||
chr7:95528558 | C | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0017others(36): Show | 42 | HG00423.hp1 HG01081.hp2 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.978+255C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528558 | ||||||
chr7:95528623 | G | A | 22 | a0001c0001t0001g0293a0001c0001t0004g0085a0001c0001t0004g0086others(19): Show | 22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+320G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528623 | ||||||
chr7:95528659 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.978+356T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528659 | ||||||
chr7:95528670 | C | T | 4 | a0001c0001t0011g0020a0001c0001t0011g0021a0001c0001t0011g0041others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+367C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528670 | ||||||
chr7:95528693 | T | C | 3 | a0001c0001t0013g0195a0001c0001t0013g0196a0001c0001t0013g0197 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.978+390T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528693 | ||||||
chr7:95528988 | G | A | 7 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0005g0024others(4): Show | 7 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+685G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95528988 | ||||||
chr7:95529071 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.978+768C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529071 | ||||||
chr7:95529142 | T | C | 3 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0302 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.978+839T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529142 | ||||||
chr7:95529221 | T | A | 4 | a0001c0001t0003g0377a0001c0001t0012g0378a0001c0001t0012g0379others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+918T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529221 | ||||||
chr7:95529258 | A | C | 1 | a0001c0001t0013g0196 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.978+955A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529258 | ||||||
chr7:95529398 | G | A | 22 | a0001c0001t0001g0293a0001c0001t0004g0085a0001c0001t0004g0086others(19): Show | 22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+1095G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529398 | ||||||
chr7:95529423 | G | A | 1 | a0001c0001t0025g0268 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.978+1120G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529423 | ||||||
chr7:95529542 | T | C | 22 | a0001c0001t0001g0293a0001c0001t0004g0085a0001c0001t0004g0086others(19): Show | 22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+1239T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529542 | ||||||
chr7:95529554 | T | A | 1 | a0001c0001t0002g0150 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.978+1251T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529554 | ||||||
chr7:95529641 | A | T | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.978+1338A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529641 | ||||||
chr7:95529651 | A | G | 4 | a0001c0001t0011g0020a0001c0001t0011g0021a0001c0001t0011g0041others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+1348A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529651 | ||||||
chr7:95529706 | G | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(58): Show | 62 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.978+1403G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529706 | ||||||
chr7:95529806 | G | A | 331 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.978+1503G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529806 | ||||||
chr7:95529869 | G | A | 12 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0005g0024others(9): Show | 12 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+1566G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529869 | ||||||
chr7:95529998 | C | A | 3 | a0001c0001t0003g0377a0001c0001t0012g0378a0002c0002t0012g0030 | 3 | HG02818.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.978+1695C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95529998 | ||||||
chr7:95530009 | A | G | 3 | a0001c0001t0013g0195a0001c0001t0013g0196a0001c0001t0013g0197 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.978+1706A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530009 | ||||||
chr7:95530038 | A | C | 1 | a0001c0001t0003g0376 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978+1735A>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530038 | ||||||
chr7:95530062 | A | G | 5 | a0001c0001t0010g0182a0001c0001t0010g0185a0001c0001t0010g0186others(2): Show | 5 | HG01192.hp1 HG01358.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+1759A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530062 | ||||||
chr7:95530105 | C | CA | 13 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0322others(10): Show | 13 | HG01433.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+1817dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530105 | C | CAAAAA | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0300others(4): Show | 7 | HG00741.hp2 HG02647.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.978+1813_978+1817d others(7): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530105 | C | CAAAAAA | 21 | a0001c0001t0001g0027a0001c0001t0001g0183a0001c0001t0001g0184others(18): Show | 21 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+1812_978+1817d others(8): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530105 | C | CAAAAAAA | 26 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0164others(23): Show | 26 | HG00438.hp2 HG01192.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.978+1811_978+1817d others(9): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530105 | C | CAAAAAAA others(1): Show |
152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.978+1810_978+1817d others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530105 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0181a0001c0001t0001g0210a0001c0001t0001g0222others(3): Show | 6 | HG00621.hp2 HG01261.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+1809_978+1817d others(11): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95530105 | |||||
chr7:95530372 | G | C | 12 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0005g0024others(9): Show | 12 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+2069G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530372 | ||||||
chr7:95530451 | C | A | 16 | a0001c0001t0004g0110a0001c0001t0004g0257a0001c0001t0004g0259others(13): Show | 16 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.978+2148C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530451 | ||||||
chr7:95530479 | A | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(19): Show | 22 | HG00639.hp1 HG00741.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.978+2176A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530479 | ||||||
chr7:95530555 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.978+2252T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530555 | ||||||
chr7:95530561 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.978+2258G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530561 | ||||||
chr7:95530940 | T | C | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG02040.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+2637T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530940 | ||||||
chr7:95530995 | G | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(58): Show | 62 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.978+2692G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95530995 | ||||||
chr7:95531284 | G | C | 1 | a0001c0001t0015g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.978+2981G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531284 | ||||||
chr7:95531334 | C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3031C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531334 | ||||||
chr7:95531541 | C | T | 60 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.978+3238C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531541 | ||||||
chr7:95531693 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.978+3390C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531693 | ||||||
chr7:95531893 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.978+3590T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531893 | ||||||
chr7:95531990 | T | C | 2 | a0002c0002t0004g0028a0002c0002t0004g0029 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.978+3687T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95531990 | ||||||
chr7:95532013 | G | A | 4 | a0001c0001t0003g0014a0001c0001t0003g0090a0001c0001t0003g0091others(1): Show | 4 | HG01255.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+3710G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532013 | ||||||
chr7:95532039 | G | A | 5 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0013g0195others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+3736G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532039 | ||||||
chr7:95532108 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.978+3805A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532108 | ||||||
chr7:95532133 | G | A | 2 | a0001c0001t0003g0121a0001c0001t0003g0122 | 2 | NA18999.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.978+3830G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532133 | ||||||
chr7:95532160 | C | T | 3 | a0001c0001t0001g0347a0002c0002t0006g0031a0002c0002t0006g0032 | 3 | HG01981.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.978+3857C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532160 | ||||||
chr7:95532341 | C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(90): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.978+4038C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532341 | ||||||
chr7:95532348 | A | G | 22 | a0001c0001t0001g0293a0001c0001t0004g0085a0001c0001t0004g0086others(19): Show | 22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.978+4045A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532348 | ||||||
chr7:95532417 | C | T | 1 | a0001c0001t0007g0374 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.979-4020C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532417 | ||||||
chr7:95532418 | G | A | 2 | a0001c0001t0001g0229a0001c0001t0005g0289 | 2 | HG01891.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.979-4019G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532418 | ||||||
chr7:95532510 | C | T | 3 | a0001c0001t0013g0195a0001c0001t0013g0196a0001c0001t0013g0197 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.979-3927C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532510 | ||||||
chr7:95532511 | G | A | 13 | a0001c0001t0004g0023a0001c0001t0004g0319a0001c0001t0004g0320others(10): Show | 13 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-3926G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532511 | ||||||
chr7:95532517 | C | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(333): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.979-3920C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532517 | ||||||
chr7:95532698 | A | G | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(332): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.979-3739A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532698 | ||||||
chr7:95532725 | G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-3712G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532725 | ||||||
chr7:95532951 | C | T | 5 | a0001c0001t0009g0019a0001c0001t0009g0250a0001c0001t0009g0260others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-3486C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95532951 | ||||||
chr7:95533175 | A | G | 3 | a0001c0001t0001g0063a0001c0001t0001g0353a0001c0001t0001g0355 | 3 | HG00280.hp2 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.979-3262A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533175 | ||||||
chr7:95533345 | A | T | 1 | a0003c0005t0001g0354 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.979-3092A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533345 | ||||||
chr7:95533347 | G | A | 1 | a0001c0001t0007g0339 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.979-3090G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533347 | ||||||
chr7:95533366 | C | T | 1 | a0001c0001t0005g0380 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.979-3071C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533366 | ||||||
chr7:95533400 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.979-3037C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533400 | ||||||
chr7:95533505 | A | G | 1 | a0001c0001t0002g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.979-2932A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533505 | ||||||
chr7:95533557 | T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0138 | 2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.979-2880T>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533557 | ||||||
chr7:95533562 | A | G | 2 | a0001c0001t0009g0260a0001c0001t0009g0296 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.979-2875A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533562 | ||||||
chr7:95533566 | C | T | 3 | a0001c0001t0012g0378a0001c0001t0012g0379a0002c0002t0012g0030 | 3 | HG02818.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.979-2871C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533566 | ||||||
chr7:95533601 | T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-2836T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533601 | ||||||
chr7:95533696 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.979-2741A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533696 | ||||||
chr7:95533883 | G | A | 27 | a0001c0001t0001g0293a0001c0001t0004g0011a0001c0001t0004g0013others(24): Show | 27 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.979-2554G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533883 | ||||||
chr7:95533889 | A | G | 1 | a0001c0001t0004g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-2548A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533889 | ||||||
chr7:95533921 | T | C | 1 | a0001c0001t0004g0338 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979-2516T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95533921 | ||||||
chr7:95534029 | G | A | 3 | a0001c0001t0005g0192a0001c0001t0005g0286a0001c0001t0005g0299 | 3 | HG02559.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.979-2408G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534029 | ||||||
chr7:95534070 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.979-2367C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534070 | ||||||
chr7:95534071 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.979-2366G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534071 | ||||||
chr7:95534072 | C | CGGTGGCC others(1): Show |
22 | a0001c0001t0001g0293a0001c0001t0004g0085a0001c0001t0004g0086others(19): Show | 22 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.979-2359_979-2358i others(10): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534072 | |||||
chr7:95534073 | G | A | 6 | a0001c0001t0007g0255a0001c0001t0007g0258a0001c0001t0007g0284others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-2364G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534073 | ||||||
chr7:95534174 | G | A | 7 | a0001c0001t0011g0020a0001c0001t0011g0021a0001c0001t0011g0041others(4): Show | 7 | HG02818.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-2263G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534174 | ||||||
chr7:95534206 | G | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(108): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.979-2231G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534206 | ||||||
chr7:95534304 | T | C | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0076 | 3 | HG02257.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-2133T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534304 | ||||||
chr7:95534328 | C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0221 | 2 | NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.979-2109C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534328 | ||||||
chr7:95534341 | T | TA | 7 | a0001c0001t0001g0329a0001c0001t0003g0045a0001c0001t0003g0052others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-2084dupA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534341 | |||||
chr7:95534341 | TA | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.979-2084delA | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95534341 | |||||
chr7:95534571 | C | T | 7 | a0001c0001t0011g0020a0001c0001t0011g0021a0001c0001t0011g0041others(4): Show | 7 | HG02818.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-1866C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534571 | ||||||
chr7:95534699 | C | T | 1 | a0001c0001t0025g0268 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.979-1738C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534699 | ||||||
chr7:95534753 | C | T | 1 | a0001c0001t0005g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.979-1684C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534753 | ||||||
chr7:95534767 | G | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(154): Show | 161 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.979-1670G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534767 | ||||||
chr7:95534894 | A | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0084a0002c0002t0003g0371 | 3 | HG02451.hp1 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.979-1543A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534894 | ||||||
chr7:95534965 | C | T | 40 | a0001c0001t0001g0293a0001c0001t0004g0011a0001c0001t0004g0013others(37): Show | 40 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1472C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95534965 | ||||||
chr7:95535021 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.979-1416C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535021 | ||||||
chr7:95535067 | T | C | 1 | a0001c0001t0003g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.979-1370T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535067 | ||||||
chr7:95535084 | G | C | 2 | a0001c0001t0017g0282a0001c0001t0017g0291 | 2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.979-1353G>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535084 | ||||||
chr7:95535101 | G | T | 1 | a0001c0001t0001g0323 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.979-1336G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535101 | ||||||
chr7:95535132 | C | G | 2 | a0001c0001t0004g0011a0001c0001t0004g0013 | 2 | HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.979-1305C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535132 | ||||||
chr7:95535145 | G | T | 2 | a0001c0001t0014g0098a0001c0001t0014g0104 | 2 | HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.979-1292G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535145 | ||||||
chr7:95535327 | G | A | 1 | a0001c0001t0008g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.979-1110G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535327 | ||||||
chr7:95535360 | T | C | 2 | a0001c0001t0015g0113a0001c0001t0015g0318 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.979-1077T>C | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535360 | ||||||
chr7:95535419 | TGATTTAT others(7): Show |
T | 30 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0085others(27): Show | 30 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.979-1015_979-1002d others(16): Show |
ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 95535419 | |||||
chr7:95535435 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.979-1002A>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535435 | ||||||
chr7:95535595 | G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-842G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535595 | ||||||
chr7:95535659 | G | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-778G>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535659 | ||||||
chr7:95535962 | C | T | 104 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(101): Show | 108 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.979-475C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95535962 | ||||||
chr7:95536258 | C | A | 1 | a0001c0001t0004g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.979-179C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 3/4 | chr7 | 95536258 | ||||||
chr7:95536585 | A | G | 1 | a0001c0001t0007g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1092+35A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536585 | ||||||
chr7:95536661 | G | A | 11 | a0001c0001t0006g0133a0001c0001t0006g0155a0001c0001t0006g0283others(8): Show | 11 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1092+111G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536661 | ||||||
chr7:95536842 | C | G | 1 | a0001c0001t0001g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1092+292C>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536842 | ||||||
chr7:95536910 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1092+360C>T | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95536910 | ||||||
chr7:95537038 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1092+488A>G | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537038 | ||||||
chr7:95537123 | G | A | 1 | a0002c0002t0006g0372 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1093-448G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537123 | ||||||
chr7:95537124 | G | A | 13 | a0001c0001t0005g0024a0001c0001t0005g0025a0001c0001t0005g0026others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093-447G>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537124 | ||||||
chr7:95537254 | C | A | 28 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0085others(25): Show | 28 | HG00621.hp1 HG00735.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1093-317C>A | ASB4 | ENSG00000005981.13 | transcript | ENST00000325885.6 | protein_coding | 4/4 | chr7 | 95537254 |