geneid | 3308 |
---|---|
ensemblid | ENSG00000170606.16 |
hgncid | 5237 |
symbol | HSPA4 |
name | heat shock protein family A (Hsp70) member 4 |
refseq_nuc | NM_002154.4 |
refseq_prot | NP_002145.3 |
ensembl_nuc | ENST00000304858.7 |
ensembl_prot | ENSP00000302961.2 |
mane_status | MANE Select |
chr | chr5 |
start | 133052013 |
end | 133106449 |
strand | + |
ver | v1.2 |
region | chr5:133052013-133106449 |
region5000 | chr5:133047013-133111449 |
regionname0 | HSPA4_chr5_133052013_133106449 |
regionname5000 | HSPA4_chr5_133047013_133111449 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 840 | 349 | 82 | 68 | 153 | 12 | 32 | 116 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0002 | 0/0 | 840 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0003 | 0/0 | 840 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0004 | 0/0 | 840 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0005 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0006 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0007 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0008 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0009 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0010 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2523 | 279 | 59 | 52 | 134 | 8 | 24 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0002 | 0/0 | 2523 | 62 | 16 | 15 | 19 | 4 | 8 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0003 | 0/0 | 2523 | 4 | 1 | 2 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0004 | 0/0 | 2523 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0005 | 0/0 | 2523 | 3 | 0 | 0 | 0 | 0 | 3 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0006 | 0/0 | 2523 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0007 | 0/0 | 2523 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0008 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0009 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0010 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0011 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0012 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0013 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0014 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
c0015 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2252 | 42 | 5 | 9 | 15 | 3 | 8 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0002 | 0/0 | 2239 | 37 | 7 | 9 | 12 | 3 | 6 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0003 | 0/0 | 2241 | 36 | 5 | 1 | 30 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0004 | 0/0 | 2253 | 27 | 4 | 9 | 11 | 1 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0005 | 0/0 | 2245 | 23 | 1 | 5 | 15 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0006 | 0/0 | 2246 | 17 | 1 | 7 | 6 | 1 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0007 | 0/0 | 2254 | 16 | 1 | 3 | 10 | 1 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0008 | 0/0 | 2252 | 14 | 10 | 1 | 1 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0009 | 0/0 | 2251 | 11 | 7 | 3 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0010 | 0/0 | 2255 | 10 | 3 | 0 | 5 | 1 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0011 | 0/0 | 2240 | 10 | 5 | 2 | 3 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0012 | 0/0 | 2250 | 9 | 2 | 3 | 1 | 0 | 3 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0013 | 0/0 | 2251 | 8 | 1 | 1 | 4 | 1 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0014 | 0/0 | 2242 | 6 | 0 | 1 | 5 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0015 | 0/0 | 2249 | 5 | 1 | 3 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0016 | 0/0 | 2247 | 4 | 0 | 0 | 2 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0017 | 0/0 | 2254 | 4 | 2 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0018 | 0/0 | 2254 | 4 | 0 | 0 | 3 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0019 | 0/0 | 2234 | 3 | 1 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0020 | 0/0 | 2253 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0021 | 0/0 | 2242 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0022 | 0/0 | 2253 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0023 | 0/0 | 2241 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0024 | 0/0 | 2232 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0025 | 0/0 | 2239 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0026 | 0/0 | 2257 | 2 | 0 | 1 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0027 | 0/0 | 2246 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0028 | 0/0 | 2251 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0029 | 0/0 | 2239 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0030 | 0/0 | 2240 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0031 | 0/0 | 2236 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0032 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0033 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0034 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0035 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0036 | 0/0 | 2246 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0037 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0038 | 0/0 | 2236 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0039 | 0/0 | 2239 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0040 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0041 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0042 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0043 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0044 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0045 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0046 | 0/0 | 2258 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0047 | 0/0 | 2264 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0048 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0049 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0050 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0051 | 0/0 | 2240 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0052 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0053 | 0/0 | 2239 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0054 | 0/0 | 2240 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0055 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0056 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0057 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0058 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0059 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0060 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0061 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0062 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0063 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0064 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0065 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0066 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0067 | 0/0 | 2251 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0068 | 0/0 | 2239 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0069 | 0/0 | 2239 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0070 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0071 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0072 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0073 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0074 | 0/0 | 2240 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0075 | 0/0 | 2239 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0076 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0077 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0078 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0079 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0080 | 0/0 | 2240 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0081 | 0/0 | 2239 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0082 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
t0083 | 0/0 | 2239 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2523 | 279 | 59 | 52 | 134 | 8 | 24 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002 | 0/0 | 2523 | 62 | 16 | 15 | 19 | 4 | 8 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0004 | 0/0 | 2523 | 4 | 4 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0007 | 0/0 | 2523 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0011 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0015 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0002c0003 | 0/0 | 2523 | 4 | 1 | 2 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0003c0005 | 0/0 | 2523 | 3 | 0 | 0 | 0 | 0 | 3 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0004c0006 | 0/0 | 2523 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0005c0009 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0006c0010 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0007c0014 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0008c0013 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0009c0012 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0010c0008 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4774 | 41 | 4 | 9 | 15 | 3 | 8 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0002 | 0/0 | 4761 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0003 | 0/0 | 4763 | 35 | 4 | 1 | 30 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0004 | 0/0 | 4775 | 24 | 2 | 9 | 10 | 1 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0005 | 0/0 | 4767 | 23 | 1 | 5 | 15 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0006 | 0/0 | 4768 | 17 | 1 | 7 | 6 | 1 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0007 | 0/0 | 4776 | 16 | 1 | 3 | 10 | 1 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0008 | 0/0 | 4774 | 14 | 10 | 1 | 1 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0009 | 0/0 | 4773 | 8 | 5 | 3 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0010 | 0/0 | 4777 | 10 | 3 | 0 | 5 | 1 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0012 | 0/0 | 4772 | 5 | 1 | 2 | 1 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0013 | 0/0 | 4773 | 7 | 1 | 1 | 4 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0014 | 0/0 | 4764 | 6 | 0 | 1 | 5 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0015 | 0/0 | 4771 | 5 | 1 | 3 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0016 | 0/0 | 4769 | 4 | 0 | 0 | 2 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0017 | 0/0 | 4776 | 4 | 2 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0018 | 0/0 | 4776 | 4 | 0 | 0 | 3 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0019 | 0/0 | 4756 | 3 | 1 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0020 | 0/0 | 4775 | 3 | 2 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0022 | 0/0 | 4775 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0023 | 0/0 | 4763 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0024 | 0/0 | 4754 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0025 | 0/0 | 4761 | 2 | 2 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0027 | 0/0 | 4768 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0028 | 0/0 | 4773 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0032 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0033 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0034 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0035 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0036 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0037 | 0/0 | 4771 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0038 | 0/0 | 4758 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0039 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0040 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0041 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0042 | 0/0 | 4769 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0043 | 0/0 | 4767 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0044 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0045 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0047 | 0/0 | 4786 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0048 | 0/0 | 4789 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0049 | 0/0 | 4753 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0050 | 0/0 | 4764 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0051 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0052 | 0/0 | 4763 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0053 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0054 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0056 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0057 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0058 | 0/0 | 4763 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0059 | 0/0 | 4767 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0060 | 0/0 | 4769 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0061 | 0/0 | 4767 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0062 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0063 | 0/0 | 4763 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0064 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0065 | 0/0 | 4777 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0066 | 0/0 | 4772 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0067 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0072 | 0/0 | 4769 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0074 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0001t0082 | 0/0 | 4765 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0002 | 0/0 | 4761 | 36 | 7 | 8 | 12 | 3 | 6 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0011 | 0/0 | 4762 | 10 | 5 | 2 | 3 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0029 | 0/0 | 4761 | 2 | 0 | 0 | 2 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0030 | 0/0 | 4762 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0031 | 0/0 | 4758 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0068 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0069 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0075 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0076 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0077 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0078 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0079 | 0/0 | 4757 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0080 | 0/0 | 4762 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0081 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0002t0083 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0004t0021 | 0/0 | 4764 | 3 | 3 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0004t0070 | 0/0 | 4763 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0007t0012 | 0/0 | 4772 | 2 | 1 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0011t0004 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0001c0015t0071 | 0/0 | 4765 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0002c0003t0026 | 0/0 | 4779 | 2 | 0 | 1 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0002c0003t0046 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0002c0003t0055 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0003c0005t0009 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0003c0005t0012 | 0/0 | 4772 | 2 | 0 | 0 | 0 | 0 | 2 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0004c0006t0001 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0004c0006t0004 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0005c0009t0004 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0006c0010t0009 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0007c0014t0009 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0008c0013t0003 | 0/0 | 4763 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0009c0012t0013 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
a0010c0008t0073 | 0/0 | 4763 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | copy fasta | chr5 | 133047013 | 133111449 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0007g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0010g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0012g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0013g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0014g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0015g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0016g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0017g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0017g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0017g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0017g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0018g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0018g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0018g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0018g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0019g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0019g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0020g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0020g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0020g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0022g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0022g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0023g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0023g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0024g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0024g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0025g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0025g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0027g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0027g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0028g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0028g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0032g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0033g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0034g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0035g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0036g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0037g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0038g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0039g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0040g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0041g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0042g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0043g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0044g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0045g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0047g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0048g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0049g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0050g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0051g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0052g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0053g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0054g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0056g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0057g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0058g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0059g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0060g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0061g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0062g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0063g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0064g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0065g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0066g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0067g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0072g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0074g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0001t0082g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0029g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0029g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0030g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0031g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0031g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0068g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0069g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0075g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0076g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0077g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0078g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0079g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0080g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0081g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0002t0083g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0021g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0021g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0004t0070g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0007t0012g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0007t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0011t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0001c0015t0071g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0026g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0026g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0046g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0002c0003t0055g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0012g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0003c0005t0012g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0004c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0004c0006t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0005c0009t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0006c0010t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0007c0014t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0008c0013t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0009c0012t0013g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
a0010c0008t0073g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0282 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0050 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0255 | EUR | GBR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00280 | hp1 | a0001 | c0001 | t0018 | g0285 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0005 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00323 | hp2 | a0001 | c0002 | t0075 | g0027 | EUR | FIN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00408 | hp2 | a0001 | c0001 | t0013 | g0263 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00438 | hp2 | a0005 | c0009 | t0004 | g0293 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00544 | hp1 | a0001 | c0001 | t0040 | g0228 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00609 | hp1 | a0001 | c0001 | t0034 | g0327 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00621 | hp1 | a0001 | c0001 | t0007 | g0322 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00621 | hp2 | a0001 | c0002 | t0011 | g0068 | EAS | CHS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0302 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00639 | hp2 | a0001 | c0002 | t0031 | g0040 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0201 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG00642 | hp2 | a0001 | c0002 | t0011 | g0052 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01069 | hp2 | a0001 | c0001 | t0017 | g0353 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01070 | hp1 | a0001 | c0001 | t0015 | g0171 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01071 | hp1 | a0001 | c0001 | t0015 | g0169 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01071 | hp2 | a0001 | c0001 | t0017 | g0354 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0250 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01074 | hp2 | a0002 | c0003 | t0046 | g0152 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0288 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0166 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0185 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0170 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01106 | hp2 | a0001 | c0001 | t0008 | g0176 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01167 | hp1 | a0001 | c0001 | t0014 | g0128 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01167 | hp2 | a0001 | c0002 | t0031 | g0024 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0290 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01168 | hp2 | a0001 | c0001 | t0028 | g0256 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01169 | hp1 | a0001 | c0002 | t0079 | g0056 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01169 | hp2 | a0001 | c0001 | t0028 | g0257 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01175 | hp1 | a0002 | c0003 | t0026 | g0159 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0339 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01243 | hp2 | a0001 | c0001 | t0024 | g0082 | AMR | PUR | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0336 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01256 | hp1 | a0001 | c0002 | t0030 | g0001 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0163 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01258 | hp2 | a0001 | c0002 | t0030 | g0001 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0296 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0173 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0298 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01496 | hp1 | a0001 | c0007 | t0012 | g0142 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01496 | hp2 | a0001 | c0002 | t0011 | g0020 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01515 | hp1 | a0009 | c0012 | t0013 | g0287 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0065 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01516 | hp1 | a0010 | c0008 | t0073 | g0016 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0174 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0330 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01934 | hp2 | a0001 | c0001 | t0009 | g0168 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01952 | hp1 | a0001 | c0001 | t0020 | g0358 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0301 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0340 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0165 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0037 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02027 | hp1 | a0001 | c0002 | t0029 | g0022 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02027 | hp2 | a0001 | c0001 | t0007 | g0258 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02055 | hp2 | a0001 | c0004 | t0021 | g0012 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02056 | hp1 | a0001 | c0001 | t0014 | g0106 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02056 | hp2 | a0001 | c0001 | t0060 | g0346 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02074 | hp2 | a0001 | c0001 | t0010 | g0289 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0348 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02132 | hp1 | a0001 | c0001 | t0010 | g0187 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02145 | hp1 | a0001 | c0002 | t0011 | g0030 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0344 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0304 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CDX | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02155 | hp2 | a0001 | c0001 | t0059 | g0240 | EAS | CDX | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02257 | hp2 | a0001 | c0002 | t0011 | g0057 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02258 | hp1 | a0004 | c0006 | t0001 | g0211 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02280 | hp1 | a0001 | c0001 | t0024 | g0080 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02280 | hp2 | a0001 | c0001 | t0033 | g0148 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02523 | hp1 | a0001 | c0001 | t0023 | g0270 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | KHV | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02572 | hp1 | a0001 | c0001 | t0064 | g0018 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02572 | hp2 | a0001 | c0002 | t0011 | g0051 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0355 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02615 | hp2 | a0008 | c0013 | t0003 | g0129 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0224 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0149 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0084 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0137 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0252 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02683 | hp2 | a0003 | c0005 | t0009 | g0164 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02698 | hp1 | a0001 | c0001 | t0039 | g0347 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02698 | hp2 | a0002 | c0003 | t0026 | g0153 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02717 | hp2 | a0001 | c0002 | t0068 | g0053 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02735 | hp1 | a0001 | c0001 | t0012 | g0175 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02735 | hp2 | a0001 | c0002 | t0081 | g0067 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02738 | hp1 | a0001 | c0002 | t0080 | g0039 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0324 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02818 | hp1 | a0001 | c0001 | t0074 | g0019 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0350 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02896 | hp1 | a0001 | c0002 | t0011 | g0029 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02896 | hp2 | a0001 | c0001 | t0020 | g0140 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02922 | hp1 | a0001 | c0004 | t0070 | g0010 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02970 | hp1 | a0001 | c0004 | t0021 | g0009 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02970 | hp2 | a0001 | c0001 | t0067 | g0017 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0267 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0227 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03041 | hp2 | a0001 | c0001 | t0019 | g0081 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03098 | hp1 | a0001 | c0004 | t0021 | g0011 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03098 | hp2 | a0001 | c0001 | t0017 | g0352 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03139 | hp1 | a0001 | c0015 | t0071 | g0013 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0157 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03195 | hp1 | a0001 | c0011 | t0004 | g0194 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03195 | hp2 | a0001 | c0007 | t0012 | g0151 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03209 | hp1 | a0001 | c0002 | t0083 | g0003 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03225 | hp1 | a0001 | c0001 | t0051 | g0004 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0229 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03486 | hp1 | a0001 | c0001 | t0025 | g0004 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03486 | hp2 | a0001 | c0001 | t0065 | g0150 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0083 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03492 | hp2 | a0001 | c0001 | t0016 | g0338 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03516 | hp1 | a0001 | c0002 | t0069 | g0061 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0314 | AFR | ESN | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0134 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03579 | hp1 | a0001 | c0001 | t0013 | g0315 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0291 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03710 | hp1 | a0001 | c0001 | t0038 | g0276 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0343 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0311 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0248 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04115 | hp2 | a0003 | c0005 | t0012 | g0167 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0063 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0319 | SAS | BEB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0177 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | STU | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0133 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18747 | hp1 | a0001 | c0001 | t0010 | g0262 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18906 | hp1 | a0004 | c0006 | t0004 | g0239 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18940 | hp2 | a0001 | c0001 | t0018 | g0286 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0309 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0334 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0246 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18952 | hp2 | a0001 | c0001 | t0047 | g0321 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18953 | hp1 | a0001 | c0001 | t0050 | g0121 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18953 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0215 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0254 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18965 | hp2 | a0001 | c0002 | t0076 | g0062 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0307 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18972 | hp2 | a0001 | c0001 | t0019 | g0090 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18975 | hp1 | a0001 | c0001 | t0061 | g0306 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18975 | hp2 | a0001 | c0001 | t0018 | g0283 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18981 | hp2 | a0001 | c0001 | t0048 | g0342 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18984 | hp2 | a0001 | c0001 | t0044 | g0006 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18986 | hp1 | a0001 | c0001 | t0036 | g0357 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18987 | hp1 | a0001 | c0001 | t0027 | g0190 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18988 | hp1 | a0001 | c0001 | t0062 | g0232 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18988 | hp2 | a0001 | c0001 | t0018 | g0284 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18989 | hp1 | a0001 | c0001 | t0052 | g0112 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18989 | hp2 | a0001 | c0001 | t0013 | g0326 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18990 | hp1 | a0001 | c0001 | t0010 | g0265 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18991 | hp1 | a0001 | c0001 | t0007 | g0275 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18991 | hp2 | a0001 | c0001 | t0058 | g0111 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18993 | hp1 | a0001 | c0001 | t0027 | g0345 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18993 | hp2 | a0001 | c0001 | t0057 | g0104 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18995 | hp1 | a0001 | c0001 | t0014 | g0119 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18995 | hp2 | a0001 | c0001 | t0045 | g0300 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18998 | hp1 | a0001 | c0001 | t0014 | g0117 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18998 | hp2 | a0001 | c0001 | t0016 | g0223 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19002 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0337 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19006 | hp1 | a0001 | c0001 | t0037 | g0264 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0102 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19011 | hp2 | a0001 | c0001 | t0014 | g0124 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0325 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19030 | hp1 | a0001 | c0001 | t0054 | g0139 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19043 | hp1 | a0001 | c0001 | t0025 | g0182 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19043 | hp2 | a0001 | c0002 | t0011 | g0059 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19057 | hp1 | a0001 | c0002 | t0011 | g0042 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19058 | hp2 | a0001 | c0001 | t0041 | g0122 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19060 | hp1 | a0001 | c0002 | t0029 | g0058 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19065 | hp1 | a0001 | c0001 | t0042 | g0210 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19074 | hp1 | a0001 | c0001 | t0015 | g0268 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19076 | hp1 | a0001 | c0002 | t0078 | g0023 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19076 | hp2 | a0001 | c0001 | t0023 | g0183 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19078 | hp2 | a0001 | c0001 | t0019 | g0118 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19082 | hp1 | a0001 | c0001 | t0035 | g0318 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19085 | hp2 | a0001 | c0002 | t0011 | g0047 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19088 | hp1 | a0001 | c0001 | t0043 | g0214 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19090 | hp2 | a0001 | c0001 | t0016 | g0317 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19091 | hp2 | a0001 | c0001 | t0013 | g0272 | EAS | JPT | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA19240 | hp2 | a0001 | c0001 | t0082 | g0014 | AFR | YRI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20129 | hp1 | a0001 | c0001 | t0072 | g0015 | AFR | ASW | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20129 | hp2 | a0006 | c0010 | t0009 | g0136 | AFR | ASW | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0305 | EUR | TSI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20905 | hp1 | a0003 | c0005 | t0012 | g0172 | SAS | GIH | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20905 | hp2 | a0001 | c0001 | t0013 | g0273 | SAS | GIH | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01123 | hp1 | a0001 | c0001 | t0013 | g0266 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02109 | hp1 | a0001 | c0001 | t0053 | g0135 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02109 | hp2 | a0002 | c0003 | t0055 | g0180 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02486 | hp2 | a0001 | c0001 | t0063 | g0356 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG02559 | hp2 | a0001 | c0001 | t0022 | g0303 | AFR | ACB | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03471 | hp1 | a0001 | c0001 | t0056 | g0145 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG03471 | hp2 | a0001 | c0001 | t0049 | g0179 | AFR | MSL | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG06807 | hp1 | a0001 | c0002 | t0077 | g0026 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0323 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA20300 | hp2 | a0001 | c0001 | t0020 | g0144 | AFR | USA | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA21309 | hp1 | a0001 | c0001 | t0066 | g0147 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
NA21309 | hp2 | a0007 | c0014 | t0009 | g0313 | AFR | LWK | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0244 | REF | REF | HSPA4_chr5_133047013_133111449 | HSPA4 | chr5 | 133047013 | 133111449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052287
|
T | A | 1 | a0010 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.37T>A | p.Cys13Ser | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 275/4774 | 37/2523 | 13/840 | chr5 | 133052287 | ||
chr5:133067417
|
G | A | 1 | a0005 | 1 | HG00438.hp2 | missense_variant&splice_region_variant | MODERATE | c.166G>A | p.Val56Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/19 | 404/4774 | 166/2523 | 56/840 | chr5 | 133067417 | ||
chr5:133070461
|
G | A | 1 | a0004 | 2 | HG02258.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.394G>A | p.Val132Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/19 | 632/4774 | 394/2523 | 132/840 | chr5 | 133070461 | ||
chr5:133073261
|
G | A | 1 | a0006 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.461G>A | p.Arg154Gln | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 699/4774 | 461/2523 | 154/840 | chr5 | 133073261 | ||
chr5:133073275
|
G | A | 1 | a0002 | 4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.475G>A | p.Ala159Thr | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 713/4774 | 475/2523 | 159/840 | chr5 | 133073275 | ||
chr5:133076676
|
C | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.686C>T | p.Thr229Met | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/19 | 924/4774 | 686/2523 | 229/840 | chr5 | 133076676 | ||
chr5:133092755
|
C | T | 1 | a0008 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1616C>T | p.Pro539Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/19 | 1854/4774 | 1616/2523 | 539/840 | chr5 | 133092755 | ||
chr5:133099561
|
C | G | 1 | a0003 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.1946C>G | p.Thr649Ser | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/19 | 2184/4774 | 1946/2523 | 649/840 | chr5 | 133099561 | ||
chr5:133104288
|
C | T | 1 | a0009 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2375C>T | p.Pro792Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 2613/4774 | 2375/2523 | 792/840 | chr5 | 133104288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052352
|
C | T | 1 | a0001c0015 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.102C>T | p.Cys34Cys | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 340/4774 | 102/2523 | 34/840 | chr5 | 133052352 | ||
chr5:133073253
|
A | G | 1 | a0001c0007 | 2 | HG01496.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.453A>G | p.Ala151Ala | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/19 | 691/4774 | 453/2523 | 151/840 | chr5 | 133073253 | ||
chr5:133074057
|
A | C | 1 | a0001c0004 | 4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.594A>C | p.Val198Val | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/19 | 832/4774 | 594/2523 | 198/840 | chr5 | 133074057 | ||
chr5:133076816
|
T | C | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.826T>C | p.Leu276Leu | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/19 | 1064/4774 | 826/2523 | 276/840 | chr5 | 133076816 | ||
chr5:133101839
|
C | T | 1 | a0001c0002 | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
synonymous_variant | LOW | c.2118C>T | p.Ile706Ile | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/19 | 2356/4774 | 2118/2523 | 706/840 | chr5 | 133101839 | ||
chr5:133104289
|
T | C | 1 | a0009c0012 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.2376T>C | p.Pro792Pro | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 2614/4774 | 2376/2523 | 792/840 | chr5 | 133104289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052032
|
C | A | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG02280.hp2 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-219C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 219 | chr5 | 133052032 | |||||
chr5:133052041
|
C | T | 1 | a0001c0002t0083 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-210C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/19 | 210 | chr5 | 133052041 | |||||
chr5:133104512
|
C | T | 1 | a0001c0001t0082 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 76 | chr5 | 133104512 | |||||
chr5:133104576
|
A | C | 1 | a0001c0001t0018 | 4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*140A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 140 | chr5 | 133104576 | |||||
chr5:133104593
|
C | G | 24 | a0001c0001t0002a0001c0001t0017a0001c0001t0072others(21): Show | 76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 157 | chr5 | 133104593 | |||||
chr5:133104731
|
T | C | 1 | a0001c0002t0068 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 295 | chr5 | 133104731 | |||||
chr5:133104905
|
C | T | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 469 | chr5 | 133104905 | |||||
chr5:133104935
|
G | A | 1 | a0001c0001t0034 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*499G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 499 | chr5 | 133104935 | |||||
chr5:133105064
|
G | GT | 6 | a0001c0001t0032a0001c0001t0033a0001c0001t0064others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*629dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 630 | INFO_REALIGN_3_PRIME | chr5 | 133105064 | ||||
chr5:133105296
|
G | A | 1 | a0001c0001t0022 | 2 | HG02559.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*860G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 860 | chr5 | 133105296 | |||||
chr5:133105301
|
G | A | 1 | a0001c0001t0035 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 865 | chr5 | 133105301 | |||||
chr5:133105386
|
C | T | 1 | a0001c0002t0081 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*950C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 950 | chr5 | 133105386 | |||||
chr5:133105511
|
C | T | 1 | a0001c0001t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1075 | chr5 | 133105511 | |||||
chr5:133105578
|
T | C | 1 | a0001c0002t0069 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1142 | chr5 | 133105578 | |||||
chr5:133105581
|
T | A | 1 | a0001c0002t0081 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1145T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1145 | chr5 | 133105581 | |||||
chr5:133105610
|
A | G | 18 | a0001c0001t0002a0001c0001t0017a0001c0001t0074others(15): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1174 | chr5 | 133105610 | |||||
chr5:133105766
|
A | G | 1 | a0001c0002t0080 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1330 | chr5 | 133105766 | |||||
chr5:133105782
|
A | T | 3 | a0001c0001t0027a0001c0001t0061a0001c0001t0062 | 4 | NA18975.hp1 NA18987.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1346A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1346 | chr5 | 133105782 | |||||
chr5:133105783
|
T | A | 3 | a0001c0001t0027a0001c0001t0061a0001c0001t0062 | 4 | NA18975.hp1 NA18987.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1347T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1347 | chr5 | 133105783 | |||||
chr5:133105788
|
C | T | 1 | a0001c0001t0060 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1352 | chr5 | 133105788 | |||||
chr5:133105801
|
C | T | 1 | a0001c0001t0059 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1365 | chr5 | 133105801 | |||||
chr5:133105811
|
T | G | 1 | a0001c0002t0029 | 2 | HG02027.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1375T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1375 | chr5 | 133105811 | |||||
chr5:133106089
|
TA | T | 5 | a0001c0001t0009a0002c0003t0026a0003c0005t0009others(2): Show | 13 | HG01175.hp1 HG01258.hp1 HG01346.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1666delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | INFO_REALIGN_3_PRIME | chr5 | 133106089 | ||||
chr5:133106100
|
AAATTTTT others(4): Show |
A | 1 | a0001c0001t0058 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665_*1675delAATT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1665 | chr5 | 133106100 | |||||
chr5:133106100
|
AAATTTTT others(5): Show |
A | 1 | a0001c0001t0057 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665_*1676delAATT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1665 | chr5 | 133106100 | |||||
chr5:133106101
|
A | AT | 1 | a0001c0001t0020 | 3 | HG01952.hp1 HG02896.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1665_*1666insT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AAT | A | 5 | a0001c0001t0012a0001c0001t0067a0001c0007t0012others(2): Show | 11 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1667delAT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATT | A | 2 | a0001c0001t0015a0001c0001t0066 | 6 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1668delATT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(3): Show |
A | 2 | a0001c0001t0014a0001c0001t0050 | 6 | HG02056.hp1 NA18953.hp1 NA18995.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1675delATTT others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(4): Show |
A | 2 | a0001c0001t0003a0001c0001t0052 | 32 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1676delATTT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(5): Show |
A | 2 | a0001c0001t0051a0001c0001t0054 | 2 | HG03225.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1677delATTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(6): Show |
A | 2 | a0001c0001t0025a0001c0001t0053 | 3 | HG02109.hp1 HG03486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1678delATTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(7): Show |
A | 1 | a0001c0002t0077 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1679delATTT others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(8): Show |
A | 2 | a0001c0001t0033a0001c0002t0078 | 2 | HG02280.hp2 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1680delATTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(9): Show |
A | 2 | a0001c0001t0014a0001c0001t0032 | 2 | HG01167.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1681delATTT others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(10): Show |
A | 3 | a0001c0001t0003a0001c0001t0063a0008c0013t0003 | 6 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1666_*1682delATTT others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(11): Show |
A | 1 | a0001c0001t0019 | 3 | HG03041.hp2 NA18972.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1683delATTT others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(12): Show |
A | 1 | a0001c0002t0079 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1684delATTT others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(13): Show |
A | 1 | a0001c0001t0024 | 2 | HG01243.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666_*1685delATTT others(16): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106101
|
AATTTTTT others(14): Show |
A | 1 | a0001c0001t0049 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666_*1686delATTT others(17): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106101 | |||||
chr5:133106102
|
A | AT | 6 | a0001c0001t0004a0001c0001t0022a0001c0001t0062others(3): Show | 30 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1704dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
A | ATT | 3 | a0001c0001t0007a0001c0001t0018a0001c0001t0035 | 21 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1704dupTT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
A | ATTT | 1 | a0001c0001t0010 | 10 | HG00140.hp2 HG02074.hp2 HG02132.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1702_*1704dupTTT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0047 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693_*1704dupTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0048 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1690_*1704dupTTTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
A | T | 3 | a0001c0001t0008a0001c0001t0020a0001c0001t0056 | 18 | HG01106.hp2 HG01952.hp1 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1666A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1666 | chr5 | 133106102 | |||||
chr5:133106102
|
AT | A | 4 | a0001c0001t0013a0001c0001t0028a0001c0001t0044others(1): Show | 11 | HG00408.hp2 HG01123.hp1 HG01168.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1704delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1704 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTT | A | 3 | a0001c0001t0016a0001c0001t0037a0001c0001t0060 | 6 | HG02056.hp2 HG03017.hp2 HG03492.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1700_*1704delTTTT others(1): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1700 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTT | A | 3 | a0001c0001t0006a0001c0001t0027a0001c0001t0036 | 20 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1704delTTTT others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1699 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT | A | 5 | a0001c0001t0005a0001c0001t0042a0001c0001t0043others(2): Show | 27 | HG00639.hp1 HG01069.hp1 HG01192.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1698_*1704delTTTT others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1698 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0004t0021 | 3 | HG02055.hp2 HG02970.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1695_*1704delTTTT others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1695 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(4): Show |
A | 6 | a0001c0001t0023a0001c0001t0072a0001c0001t0082others(3): Show | 7 | HG01516.hp1 HG02523.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1704delTTTT others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1694 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0040 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693_*1704delTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1693 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0039 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1692_*1704delTTTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1692 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0034a0001c0002t0011a0001c0002t0030 | 8 | HG00609.hp1 HG00642.hp2 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1691_*1704delTTTT others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1691 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(8): Show |
A | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0068others(3): Show | 11 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1690_*1704delTTTT others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1690 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0038 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689_*1704delTTTT others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1689 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106102
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0031 | 2 | HG00639.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1687_*1704delTTTT others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1687 | INFO_REALIGN_3_PRIME | chr5 | 133106102 | ||||
chr5:133106103
|
T | A | 1 | a0001c0001t0074 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1667 | chr5 | 133106103 | |||||
chr5:133106105
|
T | G | 6 | a0001c0002t0002a0001c0002t0011a0001c0002t0029others(3): Show | 40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1669T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1669 | chr5 | 133106105 | |||||
chr5:133106106
|
T | G | 1 | a0001c0001t0074 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1670T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1670 | chr5 | 133106106 | |||||
chr5:133106108
|
T | A | 1 | a0001c0001t0037 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1672 | chr5 | 133106108 | |||||
chr5:133106108
|
T | G | 6 | a0001c0002t0002a0001c0002t0011a0001c0002t0029others(3): Show | 40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1672T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1672 | chr5 | 133106108 | |||||
chr5:133106109
|
T | A | 1 | a0001c0001t0036 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1673T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1673 | chr5 | 133106109 | |||||
chr5:133106109
|
T | G | 1 | a0001c0001t0074 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1673T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1673 | chr5 | 133106109 | |||||
chr5:133106115
|
T | G | 1 | a0001c0004t0021 | 3 | HG02055.hp2 HG02970.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1679T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1679 | chr5 | 133106115 | |||||
chr5:133106116
|
T | G | 4 | a0001c0001t0072a0001c0001t0082a0001c0004t0070others(1): Show | 4 | HG02922.hp1 HG03139.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1680T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1680 | chr5 | 133106116 | |||||
chr5:133106117
|
T | A | 1 | a0001c0001t0034 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1681 | chr5 | 133106117 | |||||
chr5:133106118
|
T | G | 1 | a0001c0002t0077 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1682 | chr5 | 133106118 | |||||
chr5:133106119
|
T | G | 3 | a0001c0002t0011a0001c0002t0030a0001c0002t0078 | 8 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1683T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1683 | chr5 | 133106119 | |||||
chr5:133106120
|
T | G | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0068others(3): Show | 11 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1684T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1684 | chr5 | 133106120 | |||||
chr5:133106121
|
T | G | 1 | a0001c0002t0077 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1685 | chr5 | 133106121 | |||||
chr5:133106122
|
T | G | 3 | a0001c0002t0011a0001c0002t0030a0001c0002t0078 | 8 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1686T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1686 | chr5 | 133106122 | |||||
chr5:133106123
|
T | G | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0031others(5): Show | 14 | HG00323.hp2 HG00639.hp2 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1687T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1687 | chr5 | 133106123 | |||||
chr5:133106125
|
T | G | 1 | a0001c0002t0030 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1689 | chr5 | 133106125 | |||||
chr5:133106126
|
T | G | 5 | a0001c0002t0002a0001c0002t0029a0001c0002t0075others(2): Show | 35 | HG00140.hp1 HG00323.hp2 HG01081.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1690T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1690 | chr5 | 133106126 | |||||
chr5:133106127
|
T | G | 6 | a0001c0001t0074a0001c0002t0002a0001c0002t0011others(3): Show | 40 | HG00140.hp1 HG00621.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1691T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1691 | chr5 | 133106127 | |||||
chr5:133106128
|
T | G | 4 | a0001c0001t0074a0001c0002t0011a0001c0002t0076others(1): Show | 8 | HG00621.hp2 HG01496.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1692T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1692 | chr5 | 133106128 | |||||
chr5:133106128
|
TTTTTTTT others(6): Show |
T | 3 | a0001c0002t0002a0001c0002t0029a0001c0002t0081 | 33 | HG00140.hp1 HG01081.hp1 HG01255.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1693_*1705delTTTT others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1693 | chr5 | 133106128 | |||||
chr5:133106129
|
TTTTTTTT others(5): Show |
T | 4 | a0001c0001t0074a0001c0002t0011a0001c0002t0076others(1): Show | 8 | HG00621.hp2 HG01496.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1705delTTTT others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1694 | chr5 | 133106129 | |||||
chr5:133106133
|
T | G | 2 | a0001c0001t0041a0001c0001t0050 | 2 | NA18953.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1697T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1697 | chr5 | 133106133 | |||||
chr5:133106134
|
T | G | 2 | a0001c0001t0041a0001c0001t0050 | 2 | NA18953.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1698T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1698 | chr5 | 133106134 | |||||
chr5:133106135
|
T | G | 5 | a0001c0001t0003a0001c0001t0014a0001c0001t0019others(2): Show | 41 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1699T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1699 | chr5 | 133106135 | |||||
chr5:133106136
|
T | G | 8 | a0001c0001t0003a0001c0001t0014a0001c0001t0019others(5): Show | 44 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1700T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1700 | chr5 | 133106136 | |||||
chr5:133106137
|
T | G | 3 | a0001c0001t0024a0001c0001t0025a0001c0001t0051 | 5 | HG01243.hp2 HG02280.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1701T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1701 | chr5 | 133106137 | |||||
chr5:133106138
|
T | G | 11 | a0001c0001t0003a0001c0001t0014a0001c0001t0019others(8): Show | 49 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1702T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1702 | chr5 | 133106138 | |||||
chr5:133106139
|
T | G | 1 | a0001c0002t0077 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1703T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1703 | chr5 | 133106139 | |||||
chr5:133106140
|
T | G | 12 | a0001c0001t0003a0001c0001t0014a0001c0001t0019others(9): Show | 50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1704T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1704 | chr5 | 133106140 | |||||
chr5:133106141
|
G | GGT | 19 | a0001c0001t0002a0001c0001t0017a0001c0001t0037others(16): Show | 33 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1725_*1726dupTG | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1727 | INFO_REALIGN_3_PRIME | chr5 | 133106141 | ||||
chr5:133106141
|
G | GGTGTGT | 8 | a0001c0001t0003a0001c0001t0014a0001c0001t0063others(5): Show | 12 | HG01074.hp2 HG01167.hp1 HG01175.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1726dupTGTG others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1727 | INFO_REALIGN_3_PRIME | chr5 | 133106141 | ||||
chr5:133106141
|
G | T | 12 | a0001c0001t0003a0001c0001t0014a0001c0001t0019others(9): Show | 50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1705G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1705 | chr5 | 133106141 | |||||
chr5:133106158
|
G | T | 1 | a0001c0001t0043 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1722G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1722 | chr5 | 133106158 | |||||
chr5:133106165
|
G | A | 1 | a0001c0002t0078 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 19/19 | 1729 | chr5 | 133106165 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:133052376
|
T | G | 72 | a0001c0001t0002g0074a0001c0001t0064g0018a0001c0001t0067g0017others(69): Show | 74 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+19T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052376 | ||||||
chr5:133052395
|
A | G | 1 | a0001c0001t0020g0358 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.107+38A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052395 | ||||||
chr5:133052520
|
G | A | 1 | a0001c0001t0007g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.107+163G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052520 | ||||||
chr5:133052615
|
G | C | 1 | a0001c0001t0003g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107+258G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052615 | ||||||
chr5:133052801
|
T | C | 1 | a0001c0001t0004g0077 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.107+444T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052801 | ||||||
chr5:133052824
|
C | T | 1 | a0001c0001t0036g0357 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+467C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052824 | ||||||
chr5:133052825
|
G | T | 1 | a0001c0001t0036g0357 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+468G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052825 | ||||||
chr5:133052869
|
G | A | 2 | a0001c0002t0002g0007a0001c0002t0002g0008 | 2 | HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.107+512G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052869 | ||||||
chr5:133052980
|
A | G | 1 | a0001c0001t0063g0356 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+623A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133052980 | ||||||
chr5:133053047
|
G | C | 1 | a0001c0001t0020g0358 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.107+690G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053047 | ||||||
chr5:133053055
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107+698C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053055 | ||||||
chr5:133053104
|
C | T | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+747C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053104 | ||||||
chr5:133053107
|
C | G | 1 | a0001c0001t0001g0351 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107+750C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053107 | ||||||
chr5:133053213
|
A | G | 1 | a0001c0001t0003g0350 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+856A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053213 | ||||||
chr5:133053267
|
C | T | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+910C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053267 | ||||||
chr5:133053268
|
G | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.107+911G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053268 | ||||||
chr5:133053323
|
C | CTAT | 55 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0008others(52): Show | 57 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.107+967_107+968ins others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053323 | |||||
chr5:133053325
|
C | A | 132 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0160others(129): Show | 132 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.107+968C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053325 | ||||||
chr5:133053328
|
C | CT | 41 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0003g0181others(38): Show | 41 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.107+990dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053328 | |||||
chr5:133053328
|
C | T | 55 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0008others(52): Show | 57 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.107+971C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053328 | ||||||
chr5:133053328
|
CT | C | 9 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0005g0184others(6): Show | 9 | HG01099.hp2 HG02055.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+990delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133053328 | |||||
chr5:133053540
|
G | A | 3 | a0001c0001t0007g0186a0001c0001t0010g0187a0001c0001t0023g0183 | 3 | HG02132.hp1 HG02135.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.107+1183G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053540 | ||||||
chr5:133053550
|
A | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107+1193A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053550 | ||||||
chr5:133053587
|
C | T | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+1230C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053587 | ||||||
chr5:133053693
|
C | G | 1 | a0001c0007t0012g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+1336C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053693 | ||||||
chr5:133053827
|
A | G | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+1470A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053827 | ||||||
chr5:133053850
|
G | A | 1 | a0001c0001t0036g0357 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107+1493G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053850 | ||||||
chr5:133053893
|
C | T | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+1536C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053893 | ||||||
chr5:133053995
|
C | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.107+1638C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133053995 | ||||||
chr5:133054054
|
C | CA | 56 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0008others(53): Show | 58 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.107+1698dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133054054 | |||||
chr5:133054569
|
T | C | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.107+2212T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054569 | ||||||
chr5:133054623
|
C | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+2266C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054623 | ||||||
chr5:133054887
|
G | C | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+2530G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054887 | ||||||
chr5:133054891
|
T | C | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.107+2534T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133054891 | ||||||
chr5:133055014
|
T | C | 1 | a0001c0001t0005g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.107+2657T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055014 | ||||||
chr5:133055060
|
G | T | 149 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(146): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.107+2703G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055060 | ||||||
chr5:133055196
|
T | A | 1 | a0001c0001t0012g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.107+2839T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055196 | ||||||
chr5:133055200
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.107+2843G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055200 | ||||||
chr5:133055218
|
A | G | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2861A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055218 | ||||||
chr5:133055247
|
C | T | 1 | a0001c0001t0012g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.107+2890C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055247 | ||||||
chr5:133055307
|
A | AT | 59 | a0001c0001t0001g0006a0001c0001t0001g0292a0001c0001t0001g0294others(56): Show | 59 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.107+2981dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
A | ATT | 10 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0341others(7): Show | 10 | HG01175.hp2 HG01346.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+2980_107+2981d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
A | ATTTTTTT others(13): Show |
1 | a0002c0003t0055g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107+2962_107+2981d others(22): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
AT | A | 22 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(19): Show | 22 | HG00642.hp1 HG01069.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2981delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATT | A | 8 | a0001c0001t0008g0141a0001c0001t0009g0143a0001c0001t0020g0140others(5): Show | 8 | HG01074.hp2 HG01496.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2980_107+2981d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTT | A | 8 | a0001c0001t0008g0132a0001c0001t0008g0133a0001c0001t0008g0137others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2979_107+2981d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTT | A | 6 | a0001c0001t0003g0131a0001c0001t0008g0130a0001c0001t0025g0004others(3): Show | 6 | HG02486.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2978_107+2981d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTTT | A | 34 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(31): Show | 35 | HG00621.hp2 HG01167.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.107+2977_107+2981d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTTTT | A | 75 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0086others(72): Show | 76 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.107+2976_107+2981d others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTTTTT | A | 13 | a0001c0001t0003g0085a0001c0001t0032g0149a0001c0001t0033g0148others(10): Show | 13 | HG00323.hp2 HG01167.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2975_107+2981d others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+2974_107+2981d others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055307
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0023g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.107+2972_107+2981d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133055307 | |||||
chr5:133055357
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+3000A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055357 | ||||||
chr5:133055618
|
A | C | 1 | a0001c0001t0010g0289 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.107+3261A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055618 | ||||||
chr5:133055644
|
A | G | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+3287A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055644 | ||||||
chr5:133055730
|
A | G | 56 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0008others(53): Show | 58 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.107+3373A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055730 | ||||||
chr5:133055770
|
C | T | 63 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.107+3413C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055770 | ||||||
chr5:133055946
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+3589C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055946 | ||||||
chr5:133055950
|
C | T | 2 | a0001c0001t0004g0203a0001c0001t0007g0337 | 2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.107+3593C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055950 | ||||||
chr5:133055961
|
C | T | 7 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0131others(4): Show | 7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3604C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055961 | ||||||
chr5:133055992
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0074g0019 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.107+3635C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055992 | ||||||
chr5:133055993
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.107+3636G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133055993 | ||||||
chr5:133056009
|
T | C | 154 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(151): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.107+3652T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056009 | ||||||
chr5:133056010
|
G | A | 1 | a0001c0001t0067g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.107+3653G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056010 | ||||||
chr5:133056335
|
A | AT | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.107+3983dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133056335 | |||||
chr5:133056372
|
C | T | 1 | a0001c0002t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+4015C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056372 | ||||||
chr5:133056380
|
C | G | 2 | a0001c0001t0019g0081a0001c0001t0024g0080 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.107+4023C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056380 | ||||||
chr5:133056443
|
T | C | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+4086T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056443 | ||||||
chr5:133056642
|
A | G | 1 | a0001c0007t0012g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+4285A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056642 | ||||||
chr5:133056701
|
A | G | 153 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(150): Show | 155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.107+4344A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056701 | ||||||
chr5:133056799
|
A | G | 1 | a0001c0001t0007g0337 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.107+4442A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056799 | ||||||
chr5:133056835
|
C | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+4478C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133056835 | ||||||
chr5:133057048
|
A | G | 2 | a0001c0001t0052g0112a0001c0001t0058g0111 | 2 | NA18989.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.107+4691A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057048 | ||||||
chr5:133057102
|
A | G | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107+4745A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057102 | ||||||
chr5:133057205
|
G | A | 2 | a0002c0003t0026g0153a0002c0003t0046g0152 | 2 | HG01074.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.107+4848G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057205 | ||||||
chr5:133057356
|
G | A | 1 | a0001c0001t0005g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.107+4999G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057356 | ||||||
chr5:133057360
|
C | CT | 61 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0087others(58): Show | 61 | HG00558.hp1 HG00609.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.107+5019dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133057360 | |||||
chr5:133057360
|
C | CTT | 7 | a0001c0001t0003g0110a0001c0001t0003g0181a0001c0001t0025g0004others(4): Show | 7 | HG00438.hp1 HG03225.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+5018_107+5019d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133057360 | |||||
chr5:133057415
|
A | G | 1 | a0001c0001t0007g0336 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+5058A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057415 | ||||||
chr5:133057515
|
C | T | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+5158C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057515 | ||||||
chr5:133057531
|
C | G | 65 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.107+5174C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057531 | ||||||
chr5:133057550
|
A | G | 4 | a0001c0002t0002g0003a0001c0002t0002g0072a0001c0002t0002g0073others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+5193A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057550 | ||||||
chr5:133057584
|
T | C | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107+5227T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057584 | ||||||
chr5:133057615
|
A | G | 2 | a0001c0002t0030g0001a0001c0002t0075g0027 | 3 | HG00323.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.107+5258A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057615 | ||||||
chr5:133057648
|
A | G | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.107+5291A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057648 | ||||||
chr5:133057697
|
A | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.107+5340A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133057697 | ||||||
chr5:133058071
|
A | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107+5714A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058071 | ||||||
chr5:133058115
|
G | A | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+5758G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058115 | ||||||
chr5:133058134
|
G | C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.107+5777G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058134 | ||||||
chr5:133058143
|
G | A | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+5786G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058143 | ||||||
chr5:133058156
|
C | T | 1 | a0001c0007t0012g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+5799C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058156 | ||||||
chr5:133058404
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0251a0001c0001t0004g0252others(2): Show | 5 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+6047A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058404 | ||||||
chr5:133058495
|
C | G | 1 | a0001c0001t0009g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.107+6138C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058495 | ||||||
chr5:133058539
|
G | A | 1 | a0001c0002t0011g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.107+6182G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058539 | ||||||
chr5:133058603
|
G | A | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107+6246G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058603 | ||||||
chr5:133058678
|
C | G | 10 | a0001c0001t0009g0168a0001c0001t0009g0173a0001c0001t0012g0166others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-6302C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058678 | ||||||
chr5:133058849
|
C | T | 1 | a0001c0002t0002g0071 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108-6131C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058849 | ||||||
chr5:133058930
|
C | G | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-6050C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133058930 | ||||||
chr5:133059001
|
G | A | 2 | a0001c0002t0002g0031a0001c0002t0011g0030 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.108-5979G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059001 | ||||||
chr5:133059033
|
CAGG | C | 29 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0008g0083others(26): Show | 29 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.108-5944_108-5942d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059033 | |||||
chr5:133059138
|
A | G | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-5842A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059138 | ||||||
chr5:133059189
|
T | C | 10 | a0001c0001t0009g0168a0001c0001t0009g0173a0001c0001t0012g0166others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-5791T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059189 | ||||||
chr5:133059222
|
C | T | 4 | a0001c0001t0018g0283a0001c0001t0018g0284a0001c0001t0018g0285others(1): Show | 4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-5758C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059222 | ||||||
chr5:133059447
|
C | CA | 105 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.108-5517dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | |||||
chr5:133059447
|
C | CAA | 7 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(4): Show | 7 | HG02027.hp1 HG04184.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-5518_108-5517d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | |||||
chr5:133059447
|
CA | C | 12 | a0001c0001t0001g0320a0001c0001t0008g0138a0001c0001t0032g0149others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.108-5517delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133059447 | |||||
chr5:133059645
|
A | G | 1 | a0001c0001t0006g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.108-5335A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059645 | ||||||
chr5:133059688
|
G | A | 1 | a0001c0001t0003g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.108-5292G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059688 | ||||||
chr5:133059692
|
C | T | 1 | a0001c0001t0006g0319 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108-5288C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059692 | ||||||
chr5:133059845
|
T | G | 90 | a0001c0001t0002g0074a0001c0001t0008g0130a0001c0001t0008g0132others(87): Show | 92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-5135T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059845 | ||||||
chr5:133059874
|
C | T | 1 | a0001c0001t0024g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-5106C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059874 | ||||||
chr5:133059883
|
A | G | 2 | a0001c0001t0006g0250a0001c0001t0039g0347 | 2 | HG01074.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.108-5097A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133059883 | ||||||
chr5:133060030
|
T | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-4950T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060030 | ||||||
chr5:133060048
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-4932A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060048 | ||||||
chr5:133060068
|
C | CTTT | 64 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(61): Show | 66 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.108-4903_108-4901d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060068 | |||||
chr5:133060068
|
C | CTTTTT | 113 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0160others(110): Show | 113 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.108-4905_108-4901d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060068 | |||||
chr5:133060111
|
G | A | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-4869G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060111 | ||||||
chr5:133060191
|
T | C | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-4789T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060191 | ||||||
chr5:133060201
|
T | G | 1 | a0001c0001t0005g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.108-4779T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060201 | ||||||
chr5:133060264
|
G | A | 4 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(1): Show | 4 | NA18960.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4716G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060264 | ||||||
chr5:133060410
|
C | T | 1 | a0001c0001t0006g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.108-4570C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060410 | ||||||
chr5:133060440
|
A | G | 154 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(151): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.108-4540A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060440 | ||||||
chr5:133060607
|
C | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.108-4373C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060607 | ||||||
chr5:133060659
|
G | A | 1 | a0001c0002t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-4321G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060659 | ||||||
chr5:133060816
|
C | CT | 89 | a0001c0001t0001g0247a0001c0001t0002g0074a0001c0001t0003g0085others(86): Show | 91 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.108-4143dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | |||||
chr5:133060816
|
C | CTT | 62 | a0001c0001t0003g0076a0001c0001t0003g0086a0001c0001t0003g0088others(59): Show | 62 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.108-4144_108-4143d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | |||||
chr5:133060816
|
CT | C | 8 | a0001c0001t0001g0078a0001c0001t0001g0207a0001c0001t0004g0208others(5): Show | 8 | HG01074.hp2 HG01168.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-4143delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133060816 | |||||
chr5:133060836
|
T | TC | 4 | a0001c0004t0021g0009a0001c0004t0021g0011a0001c0004t0021g0012others(1): Show | 4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4144_108-4143i others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060836 | ||||||
chr5:133060851
|
G | C | 1 | a0001c0001t0010g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.108-4129G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133060851 | ||||||
chr5:133061088
|
G | T | 1 | a0001c0001t0023g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.108-3892G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061088 | ||||||
chr5:133061110
|
C | T | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108-3870C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061110 | ||||||
chr5:133061115
|
G | C | 1 | a0001c0002t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.108-3865G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061115 | ||||||
chr5:133061125
|
CT | C | 7 | a0001c0001t0013g0254a0001c0001t0023g0183a0001c0001t0028g0257others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-3840delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061125 | |||||
chr5:133061270
|
C | T | 1 | a0001c0002t0002g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.108-3710C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061270 | ||||||
chr5:133061278
|
A | G | 90 | a0001c0001t0002g0074a0001c0001t0008g0130a0001c0001t0008g0132others(87): Show | 92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-3702A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061278 | ||||||
chr5:133061358
|
G | A | 1 | a0001c0001t0015g0165 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.108-3622G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061358 | ||||||
chr5:133061401
|
T | C | 1 | a0001c0001t0063g0356 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-3579T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061401 | ||||||
chr5:133061429
|
C | CTACT | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-3549_108-3548i others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061429 | |||||
chr5:133061429
|
C | CTATT | 83 | a0001c0001t0002g0074a0001c0001t0008g0130a0001c0001t0008g0132others(80): Show | 85 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.108-3549_108-3548i others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133061429 | |||||
chr5:133061549
|
A | G | 23 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(20): Show | 23 | HG01496.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.108-3431A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061549 | ||||||
chr5:133061659
|
G | A | 3 | a0001c0002t0002g0038a0001c0002t0002g0070a0001c0002t0011g0020 | 3 | HG01081.hp1 HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.108-3321G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061659 | ||||||
chr5:133061898
|
T | A | 1 | a0001c0001t0054g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-3082T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061898 | ||||||
chr5:133061924
|
G | A | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-3056G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061924 | ||||||
chr5:133061930
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.108-3050G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061930 | ||||||
chr5:133061958
|
T | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-3022T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061958 | ||||||
chr5:133061975
|
G | T | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-3005G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133061975 | ||||||
chr5:133062006
|
A | T | 1 | a0001c0001t0054g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-2974A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062006 | ||||||
chr5:133062013
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-2967G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062013 | ||||||
chr5:133062397
|
C | A | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.108-2583C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062397 | ||||||
chr5:133062431
|
A | T | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-2549A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062431 | ||||||
chr5:133062437
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.108-2543G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062437 | ||||||
chr5:133062669
|
T | C | 1 | a0001c0002t0011g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.108-2311T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062669 | ||||||
chr5:133062676
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.108-2304C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062676 | ||||||
chr5:133062898
|
T | A | 1 | a0001c0001t0003g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.108-2082T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062898 | ||||||
chr5:133062912
|
A | G | 2 | a0001c0001t0003g0181a0001c0001t0014g0124 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.108-2068A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062912 | ||||||
chr5:133062939
|
G | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108-2041G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133062939 | ||||||
chr5:133063100
|
CT | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0008g0083others(28): Show | 31 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.108-1870delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133063100 | |||||
chr5:133063112
|
A | C | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-1868A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063112 | ||||||
chr5:133063289
|
A | AT | 66 | a0001c0001t0002g0074a0001c0001t0004g0316a0001c0001t0017g0352others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.108-1681dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133063289 | |||||
chr5:133063325
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.108-1655C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063325 | ||||||
chr5:133063346
|
T | G | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.108-1634T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063346 | ||||||
chr5:133063416
|
G | A | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-1564G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063416 | ||||||
chr5:133063471
|
C | T | 1 | a0001c0001t0006g0246 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.108-1509C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063471 | ||||||
chr5:133063502
|
C | T | 1 | a0001c0001t0054g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-1478C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063502 | ||||||
chr5:133063513
|
C | T | 3 | a0001c0002t0002g0050a0001c0002t0002g0069a0001c0002t0077g0026 | 3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.108-1467C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063513 | ||||||
chr5:133063575
|
C | T | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.108-1405C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063575 | ||||||
chr5:133063641
|
G | A | 1 | a0001c0001t0006g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.108-1339G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063641 | ||||||
chr5:133063651
|
T | G | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-1329T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063651 | ||||||
chr5:133063652
|
C | G | 1 | a0001c0002t0002g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.108-1328C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063652 | ||||||
chr5:133063687
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0013g0315a0001c0011t0004g0194 | 3 | HG01884.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.108-1293C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063687 | ||||||
chr5:133063728
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-1252C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063728 | ||||||
chr5:133063731
|
C | A | 1 | a0001c0002t0002g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.108-1249C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063731 | ||||||
chr5:133063887
|
G | C | 1 | a0005c0009t0004g0293 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.108-1093G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133063887 | ||||||
chr5:133064009
|
G | T | 1 | a0001c0001t0005g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.108-971G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064009 | ||||||
chr5:133064041
|
C | T | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.108-939C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064041 | ||||||
chr5:133064065
|
G | A | 361 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0078others(358): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.108-915G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064065 | ||||||
chr5:133064067
|
A | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.108-913A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064067 | ||||||
chr5:133064084
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.108-896T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064084 | ||||||
chr5:133064234
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0074g0019 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.108-746G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064234 | ||||||
chr5:133064244
|
G | T | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108-736G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064244 | ||||||
chr5:133064252
|
C | T | 90 | a0001c0001t0002g0074a0001c0001t0008g0130a0001c0001t0008g0132others(87): Show | 92 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.108-728C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064252 | ||||||
chr5:133064340
|
T | G | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-640T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064340 | ||||||
chr5:133064367
|
G | A | 3 | a0001c0002t0002g0050a0001c0002t0002g0069a0001c0002t0077g0026 | 3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.108-613G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064367 | ||||||
chr5:133064503
|
G | GA | 23 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(20): Show | 23 | HG01496.hp1 HG01516.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.108-464dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133064503 | |||||
chr5:133064503
|
GA | G | 6 | a0001c0001t0008g0083a0001c0001t0008g0176a0001c0001t0008g0177others(3): Show | 6 | HG01106.hp2 HG01258.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-464delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 133064503 | |||||
chr5:133064585
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.108-395C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064585 | ||||||
chr5:133064663
|
ATTATTTT | A | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-316_108-310del others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064663 | ||||||
chr5:133064672
|
T | A | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-308T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064672 | ||||||
chr5:133064863
|
A | G | 2 | a0001c0002t0002g0049a0001c0002t0011g0068 | 2 | HG00621.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.108-117A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 1/18 | chr5 | 133064863 | ||||||
chr5:133065168
|
T | A | 1 | a0001c0001t0074g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+131T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065168 | ||||||
chr5:133065179
|
C | T | 2 | a0001c0001t0005g0242a0001c0001t0006g0243 | 2 | NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.165+142C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065179 | ||||||
chr5:133065461
|
C | G | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+424C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065461 | ||||||
chr5:133065816
|
C | G | 2 | a0001c0001t0006g0241a0001c0001t0006g0288 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.165+779C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065816 | ||||||
chr5:133065964
|
G | T | 2 | a0001c0001t0001g0162a0001c0001t0008g0161 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.165+927G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133065964 | ||||||
chr5:133066038
|
G | A | 150 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(147): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.165+1001G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066038 | ||||||
chr5:133066174
|
G | A | 1 | a0001c0001t0054g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+1137G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066174 | ||||||
chr5:133066232
|
C | G | 1 | a0001c0001t0003g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-1185C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066232 | ||||||
chr5:133066290
|
C | T | 1 | a0001c0001t0004g0335 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.166-1127C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066290 | ||||||
chr5:133066409
|
T | C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-1008T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066409 | ||||||
chr5:133066610
|
C | T | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.166-807C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066610 | ||||||
chr5:133066675
|
AT | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-732delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066675 | |||||
chr5:133066736
|
C | CT | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0003g0113others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-664dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | |||||
chr5:133066736
|
CT | C | 22 | a0001c0001t0001g0197a0001c0001t0001g0247a0001c0001t0001g0294others(19): Show | 22 | HG01169.hp2 HG01243.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-664delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | |||||
chr5:133066736
|
CTT | C | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.166-665_166-664del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133066736 | |||||
chr5:133066742
|
T | C | 1 | a0001c0002t0002g0048 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.166-675T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066742 | ||||||
chr5:133066743
|
T | C | 61 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(58): Show | 63 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.166-674T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066743 | ||||||
chr5:133066770
|
A | G | 1 | a0001c0001t0003g0085 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-647A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066770 | ||||||
chr5:133066807
|
C | T | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-610C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066807 | ||||||
chr5:133066808
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-609A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066808 | ||||||
chr5:133066835
|
C | T | 1 | a0001c0002t0081g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.166-582C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133066835 | ||||||
chr5:133067046
|
T | C | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-371T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067046 | ||||||
chr5:133067079
|
T | C | 4 | a0001c0001t0018g0283a0001c0001t0018g0284a0001c0001t0018g0285others(1): Show | 4 | HG00280.hp1 NA18940.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-338T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067079 | ||||||
chr5:133067147
|
T | C | 1 | a0001c0001t0003g0125 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.166-270T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067147 | ||||||
chr5:133067238
|
C | T | 1 | a0001c0002t0002g0002 | 2 | HG02129.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.166-179C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067238 | ||||||
chr5:133067261
|
A | G | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-156A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067261 | ||||||
chr5:133067293
|
A | G | 1 | a0001c0001t0059g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.166-124A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067293 | ||||||
chr5:133067363
|
A | T | 1 | a0001c0001t0032g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-54A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | chr5 | 133067363 | ||||||
chr5:133067365
|
T | TA | 63 | a0001c0001t0001g0213a0001c0001t0002g0074a0001c0001t0072g0015others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.166-42dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133067365 | |||||
chr5:133067365
|
T | TAA | 8 | a0001c0002t0002g0028a0001c0002t0002g0031a0001c0002t0002g0054others(5): Show | 8 | HG00642.hp2 HG01516.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-43_166-42dupAA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 133067365 | |||||
chr5:133067617
|
A | G | 15 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0001g0328others(12): Show | 15 | HG00544.hp2 HG01192.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+60A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067617 | ||||||
chr5:133067649
|
C | T | 150 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(147): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.306+92C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067649 | ||||||
chr5:133067667
|
T | A | 149 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(146): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.306+110T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067667 | ||||||
chr5:133067710
|
T | G | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.306+153T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067710 | ||||||
chr5:133067741
|
A | G | 154 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(151): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.306+184A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067741 | ||||||
chr5:133067760
|
T | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+203T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067760 | ||||||
chr5:133067892
|
G | GT | 17 | a0001c0001t0001g0245a0001c0001t0001g0277a0001c0001t0003g0109others(14): Show | 17 | HG00642.hp1 HG01175.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.306+353dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133067892 | |||||
chr5:133067914
|
A | G | 1 | a0001c0001t0005g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.306+357A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133067914 | ||||||
chr5:133068066
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+509G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068066 | ||||||
chr5:133068135
|
C | G | 187 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0160others(184): Show | 189 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.306+578C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068135 | ||||||
chr5:133068181
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+624C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068181 | ||||||
chr5:133068195
|
A | G | 63 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.306+638A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068195 | ||||||
chr5:133068223
|
A | G | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.306+666A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068223 | ||||||
chr5:133068323
|
G | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+766G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068323 | ||||||
chr5:133068431
|
A | T | 1 | a0001c0001t0006g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.306+874A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068431 | ||||||
chr5:133068433
|
G | T | 1 | a0008c0013t0003g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.306+876G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068433 | ||||||
chr5:133068445
|
C | T | 3 | a0001c0001t0005g0311a0001c0001t0005g0312a0001c0001t0006g0238 | 3 | HG00408.hp1 HG02523.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.306+888C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068445 | ||||||
chr5:133068471
|
A | T | 150 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(147): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.306+914A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068471 | ||||||
chr5:133068660
|
T | G | 1 | a0001c0001t0027g0190 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.306+1103T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068660 | ||||||
chr5:133068769
|
TAAAG | T | 8 | a0001c0001t0066g0147a0001c0001t0072g0015a0001c0001t0082g0014others(5): Show | 8 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+1216_306+1219d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133068769 | |||||
chr5:133068784
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.306+1227G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068784 | ||||||
chr5:133068866
|
C | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+1309C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068866 | ||||||
chr5:133068872
|
TAA | T | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+1318_306+1319d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133068872 | |||||
chr5:133068903
|
C | G | 3 | a0001c0001t0007g0308a0001c0001t0007g0310a0001c0001t0010g0309 | 3 | NA18942.hp1 NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.306+1346C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133068903 | ||||||
chr5:133069043
|
C | T | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.307-1331C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069043 | ||||||
chr5:133069230
|
G | GTTCA | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.307-1141_307-1138d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133069230 | |||||
chr5:133069255
|
T | A | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.307-1119T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069255 | ||||||
chr5:133069255
|
T | C | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.307-1119T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069255 | ||||||
chr5:133069256
|
T | A | 2 | a0001c0002t0011g0029a0010c0008t0073g0016 | 2 | HG01516.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.307-1118T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069256 | ||||||
chr5:133069441
|
G | C | 20 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0008g0083others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.307-933G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069441 | ||||||
chr5:133069614
|
T | C | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-760T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069614 | ||||||
chr5:133069758
|
A | T | 2 | a0001c0002t0002g0031a0001c0002t0011g0030 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.307-616A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069758 | ||||||
chr5:133069945
|
C | G | 74 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(71): Show | 76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.307-429C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133069945 | ||||||
chr5:133070052
|
C | T | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-322C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070052 | ||||||
chr5:133070193
|
A | T | 45 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0008others(42): Show | 47 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-181A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070193 | ||||||
chr5:133070239
|
C | CT | 65 | a0001c0001t0002g0074a0001c0001t0006g0282a0001c0001t0023g0183others(62): Show | 67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.307-122dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 133070239 | |||||
chr5:133070271
|
A | G | 1 | a0001c0002t0002g0002 | 2 | HG02129.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.307-103A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070271 | ||||||
chr5:133070355
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0074g0019 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-19C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 3/18 | chr5 | 133070355 | ||||||
chr5:133070598
|
T | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.429+102T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070598 | ||||||
chr5:133070624
|
G | A | 1 | a0001c0002t0002g0033 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.429+128G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070624 | ||||||
chr5:133070730
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0009g0154a0001c0001t0009g0155others(1): Show | 4 | HG02486.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+234C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133070730 | ||||||
chr5:133070906
|
GA | G | 63 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.429+420delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133070906 | |||||
chr5:133071067
|
C | T | 1 | a0001c0002t0002g0031 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.429+571C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071067 | ||||||
chr5:133071284
|
C | CA | 74 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0001g0212others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.429+815dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | |||||
chr5:133071284
|
C | CAA | 7 | a0001c0001t0004g0077a0001c0001t0005g0295a0001c0001t0007g0258others(4): Show | 7 | HG02027.hp2 HG02647.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+814_429+815dup others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | |||||
chr5:133071284
|
CA | C | 24 | a0001c0001t0002g0074a0001c0001t0003g0126a0001c0001t0012g0084others(21): Show | 24 | HG00642.hp2 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.429+815delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | |||||
chr5:133071284
|
CAA | C | 70 | a0001c0001t0003g0091a0001c0001t0003g0092a0001c0001t0003g0093others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+814_429+815del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | |||||
chr5:133071284
|
CAAA | C | 36 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(33): Show | 36 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.429+813_429+815del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071284 | |||||
chr5:133071366
|
C | T | 78 | a0001c0001t0002g0074a0001c0001t0008g0130a0001c0001t0008g0132others(75): Show | 80 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.429+870C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071366 | ||||||
chr5:133071441
|
C | G | 1 | a0001c0001t0005g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.429+945C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071441 | ||||||
chr5:133071446
|
TCAAAAAA others(6): Show |
T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.429+959_429+971del others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133071446 | |||||
chr5:133071515
|
A | G | 1 | a0001c0002t0011g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.429+1019A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071515 | ||||||
chr5:133071601
|
C | T | 7 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0131others(4): Show | 7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+1105C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071601 | ||||||
chr5:133071605
|
C | T | 11 | a0001c0001t0008g0132a0001c0001t0008g0137a0001c0001t0008g0138others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1109C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071605 | ||||||
chr5:133071635
|
A | T | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+1139A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071635 | ||||||
chr5:133071716
|
C | T | 1 | a0001c0001t0036g0357 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.429+1220C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071716 | ||||||
chr5:133071996
|
T | C | 63 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.430-1234T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133071996 | ||||||
chr5:133072004
|
G | A | 57 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(54): Show | 57 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.430-1226G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072004 | ||||||
chr5:133072264
|
G | A | 5 | a0001c0001t0004g0259a0001c0001t0010g0255a0001c0001t0013g0266others(2): Show | 5 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-966G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072264 | ||||||
chr5:133072335
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.430-895A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072335 | ||||||
chr5:133072377
|
G | A | 1 | a0001c0001t0003g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.430-853G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072377 | ||||||
chr5:133072389
|
G | GTTGTTTT others(8): Show |
3 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0012 | 3 | HG02055.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.430-831_430-830ins others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072389 | |||||
chr5:133072392
|
G | GT | 62 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0247others(59): Show | 62 | HG00099.hp1 HG00621.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.430-815dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
G | GTT | 15 | a0001c0001t0001g0204a0001c0001t0001g0320a0001c0001t0005g0236others(12): Show | 15 | HG01167.hp2 HG01346.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-816_430-815dup others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
G | GTTT | 9 | a0001c0002t0002g0003a0001c0002t0002g0028a0001c0002t0002g0055others(6): Show | 9 | HG00639.hp2 HG01169.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-817_430-815dup others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
G | GTTTT | 29 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0008others(26): Show | 31 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.430-818_430-815dup others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
G | GTTTTT | 15 | a0001c0001t0008g0146a0001c0002t0002g0031a0001c0002t0002g0032others(12): Show | 15 | HG01993.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-819_430-815dup others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
G | T | 1 | a0001c0002t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.430-838G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072392 | ||||||
chr5:133072392
|
GT | G | 64 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(61): Show | 64 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.430-815delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072392
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-825_430-815del others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072392 | |||||
chr5:133072393
|
T | TTTTTTTG others(7): Show |
4 | a0001c0004t0021g0009a0001c0004t0021g0011a0001c0004t0070g0010others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-831_430-830ins others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072393 | |||||
chr5:133072409
|
T | G | 1 | a0001c0001t0010g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.430-821T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072409 | ||||||
chr5:133072562
|
A | AT | 9 | a0001c0001t0001g0200a0001c0001t0001g0220a0001c0001t0005g0248others(6): Show | 9 | HG01175.hp2 HG01261.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.430-652dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072562 | |||||
chr5:133072562
|
AT | A | 10 | a0001c0001t0005g0192a0001c0001t0008g0146a0001c0001t0060g0346others(7): Show | 10 | HG00438.hp2 HG01069.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.430-652delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 133072562 | |||||
chr5:133072565
|
T | TA | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430-665_430-664ins others(1): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072565 | ||||||
chr5:133072566
|
T | A | 54 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(51): Show | 54 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.430-664T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072566 | ||||||
chr5:133072673
|
C | T | 1 | a0001c0002t0081g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.430-557C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072673 | ||||||
chr5:133072760
|
A | G | 1 | a0001c0001t0012g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430-470A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072760 | ||||||
chr5:133072777
|
C | T | 1 | a0001c0001t0003g0105 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.430-453C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072777 | ||||||
chr5:133072869
|
T | G | 1 | a0001c0001t0001g0332 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.430-361T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072869 | ||||||
chr5:133072891
|
T | C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.430-339T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072891 | ||||||
chr5:133072939
|
T | C | 153 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(150): Show | 155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.430-291T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133072939 | ||||||
chr5:133073052
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-178C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 4/18 | chr5 | 133073052 | ||||||
chr5:133073341
|
C | T | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+12C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073341 | ||||||
chr5:133073382
|
A | G | 63 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.529+53A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073382 | ||||||
chr5:133073389
|
A | G | 2 | a0001c0001t0032g0149a0001c0001t0033g0148 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.529+60A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073389 | ||||||
chr5:133073564
|
G | T | 1 | a0001c0001t0057g0104 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+235G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073564 | ||||||
chr5:133073649
|
G | C | 2 | a0001c0001t0001g0328a0001c0001t0001g0333 | 2 | HG00544.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.529+320G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073649 | ||||||
chr5:133073674
|
A | G | 1 | a0001c0001t0012g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.530-319A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073674 | ||||||
chr5:133073684
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.530-309G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073684 | ||||||
chr5:133073724
|
A | G | 2 | a0001c0001t0032g0149a0001c0001t0033g0148 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.530-269A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073724 | ||||||
chr5:133073844
|
A | G | 1 | a0001c0001t0005g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.530-149A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073844 | ||||||
chr5:133073902
|
A | C | 3 | a0001c0001t0016g0223a0001c0001t0016g0317a0001c0001t0037g0264 | 3 | NA18998.hp2 NA19006.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.530-91A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073902 | ||||||
chr5:133073958
|
C | T | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.530-35C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 5/18 | chr5 | 133073958 | ||||||
chr5:133074175
|
T | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+49T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074175 | ||||||
chr5:133074184
|
G | A | 1 | a0001c0001t0072g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663+58G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074184 | ||||||
chr5:133074212
|
A | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.663+86A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074212 | ||||||
chr5:133074232
|
AC | A | 3 | a0001c0002t0031g0024a0001c0002t0031g0040a0001c0002t0079g0056 | 3 | HG00639.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.663+108delC | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133074232 | |||||
chr5:133074233
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.663+107C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074233 | ||||||
chr5:133074283
|
CT | C | 72 | a0001c0001t0002g0074a0001c0001t0010g0291a0001c0001t0014g0117others(69): Show | 74 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.663+169delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133074283 | |||||
chr5:133074292
|
T | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+166T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074292 | ||||||
chr5:133074307
|
T | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+181T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074307 | ||||||
chr5:133074341
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0004g0202 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.663+215C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074341 | ||||||
chr5:133074361
|
C | T | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+235C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074361 | ||||||
chr5:133074422
|
G | T | 2 | a0001c0001t0052g0112a0001c0001t0058g0111 | 2 | NA18989.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.663+296G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074422 | ||||||
chr5:133074439
|
C | T | 2 | a0003c0005t0012g0167a0003c0005t0012g0172 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.663+313C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074439 | ||||||
chr5:133074581
|
G | A | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+455G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074581 | ||||||
chr5:133074812
|
T | C | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663+686T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074812 | ||||||
chr5:133074822
|
T | C | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.663+696T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133074822 | ||||||
chr5:133075044
|
G | C | 1 | a0001c0001t0017g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.663+918G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075044 | ||||||
chr5:133075133
|
G | C | 1 | a0001c0001t0005g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.663+1007G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075133 | ||||||
chr5:133075139
|
T | A | 1 | a0001c0001t0006g0267 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.663+1013T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075139 | ||||||
chr5:133075376
|
T | G | 2 | a0001c0001t0082g0014a0001c0015t0071g0013 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.663+1250T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075376 | ||||||
chr5:133075430
|
C | T | 1 | a0001c0001t0072g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.664-1224C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075430 | ||||||
chr5:133075644
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1010A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075644 | ||||||
chr5:133075739
|
G | A | 154 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(151): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.664-915G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075739 | ||||||
chr5:133075769
|
A | G | 1 | a0002c0003t0026g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.664-885A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075769 | ||||||
chr5:133075848
|
TAAAG | T | 51 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(48): Show | 51 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.664-802_664-799del others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 133075848 | |||||
chr5:133075884
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-770A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075884 | ||||||
chr5:133075994
|
G | A | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.664-660G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075994 | ||||||
chr5:133075997
|
G | C | 1 | a0001c0001t0013g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664-657G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133075997 | ||||||
chr5:133076077
|
A | G | 2 | a0001c0001t0013g0254a0001c0001t0013g0272 | 2 | NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.664-577A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076077 | ||||||
chr5:133076392
|
A | T | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-262A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076392 | ||||||
chr5:133076607
|
A | G | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.664-47A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076607 | ||||||
chr5:133076650
|
T | A | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.664-4T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 6/18 | chr5 | 133076650 | ||||||
chr5:133076988
|
C | T | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+90C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133076988 | ||||||
chr5:133077156
|
C | T | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.908+258C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077156 | ||||||
chr5:133077327
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.908+429C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077327 | ||||||
chr5:133077358
|
C | T | 2 | a0001c0001t0004g0331a0001c0001t0004g0343 | 2 | HG02040.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.908+460C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077358 | ||||||
chr5:133077360
|
C | T | 4 | a0002c0003t0026g0153a0002c0003t0026g0159a0002c0003t0046g0152others(1): Show | 4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+462C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077360 | ||||||
chr5:133077394
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+496C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077394 | ||||||
chr5:133077471
|
C | T | 1 | a0001c0001t0007g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.908+573C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077471 | ||||||
chr5:133077562
|
C | T | 1 | a0001c0001t0049g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.908+664C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077562 | ||||||
chr5:133077628
|
C | T | 1 | a0001c0002t0069g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908+730C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077628 | ||||||
chr5:133077629
|
G | A | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.908+731G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077629 | ||||||
chr5:133077641
|
A | C | 1 | a0001c0001t0010g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.908+743A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077641 | ||||||
chr5:133077646
|
CT | C | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.908+749delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077646 | ||||||
chr5:133077754
|
T | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+856T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077754 | ||||||
chr5:133077884
|
T | G | 2 | a0001c0001t0003g0095a0001c0001t0003g0096 | 2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.908+986T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077884 | ||||||
chr5:133077960
|
G | C | 1 | a0001c0001t0006g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.908+1062G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133077960 | ||||||
chr5:133078039
|
G | C | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1141G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078039 | ||||||
chr5:133078061
|
G | A | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+1163G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078061 | ||||||
chr5:133078092
|
G | A | 1 | a0001c0002t0011g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.908+1194G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078092 | ||||||
chr5:133078286
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1388C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078286 | ||||||
chr5:133078346
|
A | G | 1 | a0001c0001t0004g0305 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.908+1448A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078346 | ||||||
chr5:133078462
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+1564C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078462 | ||||||
chr5:133078492
|
G | C | 1 | a0001c0002t0002g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+1594G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078492 | ||||||
chr5:133078508
|
G | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1610G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078508 | ||||||
chr5:133078634
|
CCAAAAAA | C | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1737_908+1743d others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078634 | ||||||
chr5:133078635
|
C | CA | 84 | a0001c0001t0001g0260a0001c0001t0001g0281a0001c0001t0002g0074others(81): Show | 86 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.908+1759dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | |||||
chr5:133078635
|
CA | C | 6 | a0001c0001t0001g0079a0001c0001t0003g0108a0001c0001t0009g0156others(3): Show | 6 | HG01074.hp2 HG01515.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1759delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | |||||
chr5:133078635
|
CAA | C | 15 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0137others(12): Show | 15 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.908+1758_908+1759d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | |||||
chr5:133078635
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0219 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.908+1750_908+1759d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | |||||
chr5:133078635
|
CAAAAAAA others(5): Show |
C | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+1748_908+1759d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078635 | |||||
chr5:133078668
|
A | G | 1 | a0001c0001t0038g0276 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.908+1770A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078668 | ||||||
chr5:133078686
|
C | T | 1 | a0001c0002t0011g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.908+1788C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078686 | ||||||
chr5:133078696
|
A | T | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.908+1798A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078696 | ||||||
chr5:133078732
|
ATTG | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1843_908+1845d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133078732 | |||||
chr5:133078739
|
T | C | 1 | a0001c0001t0072g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.908+1841T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078739 | ||||||
chr5:133078841
|
C | T | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.908+1943C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078841 | ||||||
chr5:133078880
|
C | T | 1 | a0001c0002t0011g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.908+1982C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133078880 | ||||||
chr5:133079090
|
T | A | 4 | a0001c0002t0002g0003a0001c0002t0002g0072a0001c0002t0002g0073others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+2192T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079090 | ||||||
chr5:133079233
|
G | A | 4 | a0001c0001t0012g0084a0001c0001t0020g0140a0001c0001t0020g0144others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+2335G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079233 | ||||||
chr5:133079442
|
G | C | 1 | a0001c0002t0002g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+2544G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079442 | ||||||
chr5:133079586
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.908+2688A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079586 | ||||||
chr5:133079637
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.908+2739A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079637 | ||||||
chr5:133079730
|
C | T | 1 | a0001c0001t0007g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.908+2832C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079730 | ||||||
chr5:133079754
|
G | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+2856G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079754 | ||||||
chr5:133079810
|
C | T | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.908+2912C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079810 | ||||||
chr5:133079877
|
A | G | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.908+2979A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133079877 | ||||||
chr5:133080188
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+3290C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080188 | ||||||
chr5:133080189
|
G | A | 4 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(1): Show | 4 | NA18960.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3291G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080189 | ||||||
chr5:133080204
|
A | G | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.908+3306A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080204 | ||||||
chr5:133080417
|
C | CA | 99 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0198others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.908+3543dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | |||||
chr5:133080417
|
C | CAA | 26 | a0001c0001t0003g0076a0001c0001t0003g0091a0001c0001t0003g0095others(23): Show | 26 | HG00438.hp1 HG00609.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.908+3542_908+3543d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | |||||
chr5:133080417
|
CAA | C | 54 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(51): Show | 56 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.908+3542_908+3543d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080417 | |||||
chr5:133080437
|
A | G | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.908+3539A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080437 | ||||||
chr5:133080442
|
C | A | 4 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3544C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080442 | ||||||
chr5:133080499
|
C | T | 1 | a0001c0002t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+3601C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080499 | ||||||
chr5:133080500
|
A | G | 7 | a0001c0002t0002g0021a0001c0002t0002g0036a0001c0002t0002g0037others(4): Show | 8 | HG00323.hp2 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+3602A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080500 | ||||||
chr5:133080569
|
G | C | 4 | a0001c0002t0002g0003a0001c0002t0002g0072a0001c0002t0002g0073others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3671G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080569 | ||||||
chr5:133080591
|
A | G | 1 | a0001c0001t0005g0235 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.908+3693A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080591 | ||||||
chr5:133080680
|
A | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | NA18974.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.908+3782A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080680 | ||||||
chr5:133080680
|
AT | A | 6 | a0001c0001t0001g0207a0001c0001t0004g0349a0001c0001t0013g0254others(3): Show | 6 | NA18964.hp1 NA18989.hp2 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+3791delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133080680 | |||||
chr5:133080682
|
T | A | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0008g0261others(9): Show | 12 | HG01243.hp2 HG02129.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.908+3784T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080682 | ||||||
chr5:133080779
|
A | G | 4 | a0001c0004t0021g0009a0001c0004t0021g0011a0001c0004t0021g0012others(1): Show | 4 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3881A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080779 | ||||||
chr5:133080785
|
A | T | 1 | a0001c0001t0006g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.908+3887A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080785 | ||||||
chr5:133080860
|
T | C | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+3962T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133080860 | ||||||
chr5:133081094
|
C | G | 1 | a0001c0001t0010g0265 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.908+4196C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081094 | ||||||
chr5:133081130
|
C | T | 50 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(47): Show | 50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.908+4232C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081130 | ||||||
chr5:133081355
|
T | C | 4 | a0001c0001t0003g0087a0001c0001t0003g0099a0001c0001t0003g0105others(1): Show | 4 | NA18944.hp2 NA18970.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+4457T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081355 | ||||||
chr5:133081492
|
G | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.908+4594G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081492 | ||||||
chr5:133081656
|
C | T | 4 | a0002c0003t0026g0153a0002c0003t0026g0159a0002c0003t0046g0152others(1): Show | 4 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+4758C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081656 | ||||||
chr5:133081830
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.908+4932G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081830 | ||||||
chr5:133081882
|
T | G | 1 | a0001c0001t0008g0178 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.909-4900T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081882 | ||||||
chr5:133081978
|
T | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-4804T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133081978 | ||||||
chr5:133082034
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-4748A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082034 | ||||||
chr5:133082150
|
G | A | 79 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(76): Show | 79 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.909-4632G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082150 | ||||||
chr5:133082232
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.909-4550C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082232 | ||||||
chr5:133082303
|
A | T | 4 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0011g0052others(1): Show | 4 | HG00642.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-4479A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082303 | ||||||
chr5:133082344
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-4438G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082344 | ||||||
chr5:133082388
|
C | G | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.909-4394C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082388 | ||||||
chr5:133082559
|
G | A | 184 | a0001c0001t0001g0160a0001c0001t0002g0074a0001c0001t0003g0076others(181): Show | 186 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.909-4223G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082559 | ||||||
chr5:133082627
|
G | A | 1 | a0001c0001t0010g0262 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.909-4155G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082627 | ||||||
chr5:133082880
|
A | G | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.909-3902A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133082880 | ||||||
chr5:133083062
|
G | C | 1 | a0001c0001t0010g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.909-3720G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083062 | ||||||
chr5:133083121
|
C | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-3661C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083121 | ||||||
chr5:133083121
|
C | T | 1 | a0001c0001t0003g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.909-3661C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083121 | ||||||
chr5:133083144
|
C | CA | 23 | a0001c0001t0001g0226a0001c0001t0003g0109a0001c0001t0003g0113others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.909-3620dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133083144 | |||||
chr5:133083144
|
C | CAA | 6 | a0001c0004t0021g0009a0001c0004t0021g0011a0001c0004t0021g0012others(3): Show | 6 | HG01175.hp1 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-3621_909-3620d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133083144 | |||||
chr5:133083163
|
T | A | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3619T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083163 | ||||||
chr5:133083165
|
A | T | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3617A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083165 | ||||||
chr5:133083166
|
C | A | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-3616C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083166 | ||||||
chr5:133083180
|
C | T | 1 | a0001c0001t0015g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.909-3602C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083180 | ||||||
chr5:133083243
|
C | T | 1 | a0001c0001t0032g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.909-3539C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083243 | ||||||
chr5:133083282
|
A | T | 67 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(64): Show | 69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.909-3500A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083282 | ||||||
chr5:133083421
|
A | G | 3 | a0001c0001t0008g0178a0001c0001t0009g0174a0001c0001t0015g0157 | 3 | HG01891.hp1 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.909-3361A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083421 | ||||||
chr5:133083597
|
G | A | 1 | a0001c0001t0022g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.909-3185G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083597 | ||||||
chr5:133083624
|
G | C | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.909-3158G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083624 | ||||||
chr5:133083691
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.909-3091C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083691 | ||||||
chr5:133083733
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.909-3049C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083733 | ||||||
chr5:133083907
|
C | T | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-2875C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133083907 | ||||||
chr5:133084033
|
A | G | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.909-2749A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084033 | ||||||
chr5:133084074
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2708A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084074 | ||||||
chr5:133084122
|
G | A | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.909-2660G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084122 | ||||||
chr5:133084137
|
T | C | 1 | a0001c0001t0010g0265 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.909-2645T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084137 | ||||||
chr5:133084257
|
T | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2525T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084257 | ||||||
chr5:133084365
|
C | T | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.909-2417C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084365 | ||||||
chr5:133084590
|
C | T | 10 | a0001c0001t0008g0083a0001c0001t0008g0161a0001c0001t0008g0176others(7): Show | 10 | HG01106.hp2 HG01258.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-2192C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084590 | ||||||
chr5:133084697
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2085C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084697 | ||||||
chr5:133084716
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909-2066C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084716 | ||||||
chr5:133084771
|
A | G | 3 | a0001c0002t0002g0036a0001c0002t0030g0001a0001c0002t0075g0027 | 4 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-2011A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084771 | ||||||
chr5:133084777
|
C | T | 1 | a0001c0001t0049g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.909-2005C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084777 | ||||||
chr5:133084800
|
A | G | 3 | a0001c0002t0002g0050a0001c0002t0002g0069a0001c0002t0077g0026 | 3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.909-1982A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084800 | ||||||
chr5:133084811
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1971C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084811 | ||||||
chr5:133084956
|
C | T | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-1826C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133084956 | ||||||
chr5:133085134
|
TA | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1639delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085134 | |||||
chr5:133085234
|
A | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1548A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085234 | ||||||
chr5:133085410
|
TGGAAGGT others(5): Show |
T | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-1371_909-1360d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085410 | ||||||
chr5:133085489
|
T | TAAAAAAA others(5): Show |
3 | a0001c0001t0012g0084a0001c0001t0020g0140a0001c0001t0056g0145 | 3 | HG02630.hp2 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.909-1291_909-1280d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(6): Show |
3 | a0001c0001t0003g0095a0001c0001t0003g0103a0001c0001t0020g0144 | 3 | HG00558.hp1 NA18945.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.909-1292_909-1280d others(15): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(7): Show |
8 | a0001c0001t0003g0087a0001c0001t0003g0099a0001c0001t0003g0105others(5): Show | 8 | HG03225.hp1 HG03486.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(16): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(8): Show |
51 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(48): Show | 53 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(17): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(9): Show |
13 | a0001c0001t0072g0015a0001c0001t0074g0019a0001c0001t0082g0014others(10): Show | 13 | HG01358.hp1 HG01433.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(18): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(11): Show |
5 | a0001c0001t0003g0120a0001c0001t0058g0111a0001c0004t0021g0011others(2): Show | 5 | HG01516.hp1 HG02055.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(20): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(12): Show |
1 | a0001c0004t0021g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(21): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0003g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(23): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.909-1280_909-1279i others(25): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(20): Show |
3 | a0001c0001t0064g0018a0001c0001t0065g0150a0001c0001t0067g0017 | 3 | HG02572.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(29): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(21): Show |
4 | a0001c0001t0014g0128a0001c0001t0032g0149a0001c0001t0033g0148others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(30): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(22): Show |
2 | a0001c0001t0003g0131a0001c0001t0066g0147 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(31): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(23): Show |
2 | a0001c0001t0054g0139a0001c0007t0012g0142 | 2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(32): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(24): Show |
2 | a0001c0001t0008g0133a0001c0001t0008g0138 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(33): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(25): Show |
9 | a0001c0001t0003g0076a0001c0001t0003g0098a0001c0001t0003g0125others(6): Show | 9 | HG00609.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(34): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(26): Show |
12 | a0001c0001t0003g0086a0001c0001t0003g0088a0001c0001t0003g0089others(9): Show | 12 | HG00438.hp1 HG02074.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(35): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(27): Show |
6 | a0001c0001t0003g0093a0001c0001t0003g0114a0001c0001t0003g0181others(3): Show | 6 | HG02109.hp1 HG02300.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(36): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(28): Show |
5 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0003g0094others(2): Show | 5 | HG02080.hp2 HG02615.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.909-1280_909-1279i others(37): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(29): Show |
2 | a0001c0001t0003g0109a0001c0001t0019g0090 | 2 | NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(38): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(30): Show |
2 | a0001c0001t0003g0116a0001c0001t0008g0141 | 2 | HG02559.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(39): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(31): Show |
3 | a0001c0001t0010g0134a0001c0001t0057g0104a0006c0010t0009g0136 | 3 | HG03540.hp1 NA18993.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(40): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(32): Show |
2 | a0001c0001t0003g0096a0001c0001t0050g0121 | 2 | NA18939.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(41): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(34): Show |
1 | a0001c0001t0014g0117 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(43): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(35): Show |
2 | a0001c0001t0014g0119a0001c0001t0052g0112 | 2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.909-1280_909-1279i others(44): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(36): Show |
1 | a0001c0001t0003g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(45): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(37): Show |
1 | a0001c0001t0014g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.909-1280_909-1279i others(46): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TAAAAAAA others(51): Show |
1 | a0001c0001t0014g0124 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.909-1280_909-1279i others(60): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085489 | |||||
chr5:133085489
|
T | TTAAAAAA others(19): Show |
3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-1293_909-1292i others(28): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085489 | ||||||
chr5:133085503
|
T | A | 1 | a0001c0001t0003g0114 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.909-1279T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085503 | ||||||
chr5:133085511
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.909-1271T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085511 | ||||||
chr5:133085519
|
C | G | 7 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0131others(4): Show | 7 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.909-1263C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085519 | ||||||
chr5:133085637
|
G | A | 1 | a0001c0015t0071g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.909-1145G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085637 | ||||||
chr5:133085689
|
A | C | 4 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-1093A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085689 | ||||||
chr5:133085737
|
GCAGGGAG others(18): Show |
G | 79 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(76): Show | 79 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.909-1013_909-989de others(26): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133085737 | |||||
chr5:133085857
|
C | T | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.909-925C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085857 | ||||||
chr5:133085980
|
G | A | 1 | a0001c0002t0002g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.909-802G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085980 | ||||||
chr5:133085987
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-795A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133085987 | ||||||
chr5:133086185
|
A | G | 1 | a0001c0002t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909-597A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086185 | ||||||
chr5:133086219
|
A | G | 1 | a0001c0001t0012g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909-563A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086219 | ||||||
chr5:133086267
|
CTCT | C | 87 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(84): Show | 87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.909-506_909-504del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 133086267 | |||||
chr5:133086298
|
G | A | 87 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(84): Show | 87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.909-484G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086298 | ||||||
chr5:133086299
|
C | T | 1 | a0001c0001t0008g0178 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.909-483C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086299 | ||||||
chr5:133086437
|
G | A | 10 | a0001c0001t0008g0083a0001c0001t0008g0161a0001c0001t0008g0176others(7): Show | 10 | HG01106.hp2 HG01258.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-345G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086437 | ||||||
chr5:133086567
|
C | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-215C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086567 | ||||||
chr5:133086580
|
G | T | 2 | a0001c0001t0032g0149a0001c0001t0033g0148 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.909-202G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086580 | ||||||
chr5:133086760
|
T | G | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-22T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086760 | ||||||
chr5:133086761
|
G | T | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.909-21G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 7/18 | chr5 | 133086761 | ||||||
chr5:133086889
|
G | A | 1 | a0001c0001t0004g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.985+31G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133086889 | ||||||
chr5:133086998
|
A | T | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.985+140A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133086998 | ||||||
chr5:133087025
|
A | T | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.985+167A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087025 | ||||||
chr5:133087133
|
C | CT | 6 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0131others(3): Show | 6 | HG01167.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+279dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 133087133 | |||||
chr5:133087151
|
G | A | 1 | a0001c0001t0067g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.985+293G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087151 | ||||||
chr5:133087194
|
G | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.985+336G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087194 | ||||||
chr5:133087309
|
T | C | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+451T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087309 | ||||||
chr5:133087397
|
C | CT | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.985+541dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 133087397 | |||||
chr5:133087575
|
C | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.985+717C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087575 | ||||||
chr5:133087587
|
C | G | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.985+729C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087587 | ||||||
chr5:133087633
|
T | A | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.986-771T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087633 | ||||||
chr5:133087634
|
A | T | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.986-770A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087634 | ||||||
chr5:133087760
|
A | C | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.986-644A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087760 | ||||||
chr5:133087772
|
C | T | 13 | a0001c0001t0005g0205a0001c0001t0005g0206a0001c0001t0005g0218others(10): Show | 13 | HG01192.hp2 HG01978.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.986-632C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087772 | ||||||
chr5:133087869
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.986-535C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133087869 | ||||||
chr5:133088020
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.986-384C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088020 | ||||||
chr5:133088063
|
C | G | 1 | a0001c0001t0005g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.986-341C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088063 | ||||||
chr5:133088072
|
T | C | 58 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0001g0217others(55): Show | 58 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.986-332T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088072 | ||||||
chr5:133088109
|
G | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.986-295G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088109 | ||||||
chr5:133088277
|
G | A | 88 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(85): Show | 88 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.986-127G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088277 | ||||||
chr5:133088354
|
T | C | 3 | a0001c0001t0009g0168a0001c0001t0009g0173a0001c0001t0012g0166 | 3 | HG01099.hp1 HG01346.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.986-50T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 8/18 | chr5 | 133088354 | ||||||
chr5:133088783
|
A | T | 1 | a0001c0001t0010g0289 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1137+228A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133088783 | ||||||
chr5:133089028
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0007g0339 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1138-27C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133089028 | ||||||
chr5:133089051
|
C | T | 50 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(47): Show | 50 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.1138-4C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 9/18 | chr5 | 133089051 | ||||||
chr5:133089259
|
A | G | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1244+98A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089259 | ||||||
chr5:133089271
|
T | C | 1 | a0001c0001t0006g0319 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1244+110T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089271 | ||||||
chr5:133089289
|
A | G | 1 | a0001c0001t0005g0297 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1244+128A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089289 | ||||||
chr5:133089357
|
A | G | 187 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0160others(184): Show | 189 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.1244+196A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089357 | ||||||
chr5:133089477
|
G | A | 87 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(84): Show | 87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1245-85G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 10/18 | chr5 | 133089477 | ||||||
chr5:133089723
|
G | GA | 80 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(77): Show | 80 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1378+42dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133089723 | |||||
chr5:133089773
|
A | G | 87 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(84): Show | 87 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1378+78A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089773 | ||||||
chr5:133089865
|
A | C | 14 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0003g0093others(11): Show | 14 | HG00558.hp1 HG02055.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378+170A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089865 | ||||||
chr5:133089866
|
A | T | 1 | a0001c0001t0004g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1378+171A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089866 | ||||||
chr5:133089907
|
C | T | 2 | a0001c0001t0001g0328a0001c0001t0001g0333 | 2 | HG00544.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1378+212C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089907 | ||||||
chr5:133089948
|
A | C | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1378+253A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133089948 | ||||||
chr5:133090012
|
T | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+317T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090012 | ||||||
chr5:133090112
|
T | C | 1 | a0001c0001t0005g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1378+417T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090112 | ||||||
chr5:133090182
|
C | G | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1378+487C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090182 | ||||||
chr5:133090219
|
G | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+524G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090219 | ||||||
chr5:133090234
|
G | C | 1 | a0001c0002t0068g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1378+539G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090234 | ||||||
chr5:133090235
|
G | T | 4 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+540G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090235 | ||||||
chr5:133090261
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1378+566C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090261 | ||||||
chr5:133090300
|
G | A | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+605G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090300 | ||||||
chr5:133090305
|
C | T | 17 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(14): Show | 17 | HG01243.hp2 HG01496.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+610C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090305 | ||||||
chr5:133090406
|
A | C | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1378+711A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090406 | ||||||
chr5:133090430
|
C | CA | 79 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(76): Show | 79 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1379-738dupA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090430
|
C | CAA | 27 | a0001c0001t0001g0220a0001c0001t0003g0086a0001c0001t0003g0120others(24): Show | 27 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1379-739_1379-738d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090430
|
C | CAAA | 43 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0003g0076others(40): Show | 43 | HG00558.hp1 HG00609.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1379-740_1379-738d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090430
|
C | CAAAA | 10 | a0001c0001t0003g0091a0001c0001t0003g0105a0001c0001t0003g0110others(7): Show | 10 | HG00438.hp1 HG02074.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-741_1379-738d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090430
|
CA | C | 17 | a0001c0001t0001g0188a0001c0001t0001g0274a0001c0001t0005g0209others(14): Show | 17 | HG00408.hp1 HG01081.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379-738delA | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090430
|
CAA | C | 51 | a0001c0001t0001g0226a0001c0002t0002g0002a0001c0002t0002g0003others(48): Show | 53 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1379-739_1379-738d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 133090430 | |||||
chr5:133090504
|
T | C | 2 | a0001c0002t0002g0050a0001c0002t0077g0026 | 2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1379-689T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090504 | ||||||
chr5:133090520
|
C | T | 1 | a0001c0007t0012g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1379-673C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090520 | ||||||
chr5:133090573
|
C | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1379-620C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090573 | ||||||
chr5:133090653
|
G | T | 1 | a0001c0001t0020g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1379-540G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090653 | ||||||
chr5:133090694
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-499C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090694 | ||||||
chr5:133090705
|
C | A | 1 | a0001c0001t0004g0203 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1379-488C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090705 | ||||||
chr5:133090734
|
C | A | 1 | a0001c0002t0002g0032 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1379-459C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090734 | ||||||
chr5:133090808
|
A | G | 17 | a0001c0001t0001g0245a0001c0001t0008g0130a0001c0001t0008g0132others(14): Show | 17 | HG01496.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-385A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090808 | ||||||
chr5:133090959
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1379-234C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133090959 | ||||||
chr5:133091159
|
GTT | G | 6 | a0001c0002t0002g0032a0001c0002t0002g0038a0001c0002t0002g0041others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1379-33_1379-32del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 11/18 | chr5 | 133091159 | ||||||
chr5:133091598
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+224C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091598 | ||||||
chr5:133091696
|
G | T | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+322G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091696 | ||||||
chr5:133091874
|
A | C | 1 | a0001c0001t0003g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1560+500A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091874 | ||||||
chr5:133091874
|
AAAC | A | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+518_1560+520d others(5): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 133091874 | |||||
chr5:133091895
|
A | C | 1 | a0001c0002t0002g0054 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1560+521A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091895 | ||||||
chr5:133091953
|
G | A | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1560+579G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133091953 | ||||||
chr5:133092025
|
T | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1560+651T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092025 | ||||||
chr5:133092042
|
C | G | 1 | a0001c0001t0040g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1561-658C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092042 | ||||||
chr5:133092057
|
CAA | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561-640_1561-639d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 133092057 | |||||
chr5:133092262
|
C | G | 1 | a0002c0003t0055g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1561-438C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092262 | ||||||
chr5:133092284
|
G | T | 2 | a0001c0002t0002g0031a0001c0002t0011g0030 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1561-416G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092284 | ||||||
chr5:133092503
|
T | G | 2 | a0001c0001t0004g0077a0001c0001t0008g0261 | 2 | NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1561-197T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092503 | ||||||
chr5:133092515
|
A | G | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561-185A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 12/18 | chr5 | 133092515 | ||||||
chr5:133092806
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0025g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1650+25_1650+26ins others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0025g0004a0001c0001t0051g0004 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1650+25_1650+26ins others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0054g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650+36_1650+49dup others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GT | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0197others(65): Show | 68 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1650+49delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTT | G | 114 | a0001c0001t0001g0005a0001c0001t0001g0188a0001c0001t0001g0207others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1650+48_1650+49del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTT | G | 41 | a0001c0001t0001g0251a0001c0001t0003g0076a0001c0001t0003g0085others(38): Show | 41 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1650+47_1650+49del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT | G | 58 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1650+43_1650+49del others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT others(1): Show |
G | 12 | a0001c0001t0002g0074a0001c0001t0008g0132a0001c0001t0009g0143others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+42_1650+49del others(8): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT others(2): Show |
G | 14 | a0001c0001t0008g0130a0001c0001t0008g0133a0001c0001t0008g0137others(11): Show | 14 | HG01496.hp1 HG01516.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1650+41_1650+49del others(9): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0072g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1650+40_1650+49del others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0006g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1650+38_1650+49del others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092806
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0006g0288a0001c0001t0006g0319 | 2 | HG01081.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1650+37_1650+49del others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092806 | |||||
chr5:133092808
|
T | G | 3 | a0001c0001t0005g0221a0001c0001t0005g0235a0001c0001t0061g0306 | 3 | NA18945.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1650+19T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092808 | ||||||
chr5:133092809
|
T | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0236a0001c0001t0027g0345 | 3 | NA18993.hp1 NA19007.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1650+20T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092809 | ||||||
chr5:133092810
|
T | G | 2 | a0001c0001t0006g0307a0001c0001t0027g0190 | 2 | NA18972.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1650+21T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092810 | ||||||
chr5:133092816
|
T | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650+27T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092816 | ||||||
chr5:133092817
|
T | C | 1 | a0001c0002t0002g0049 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1650+28T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092817 | ||||||
chr5:133092818
|
T | C | 58 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1650+29T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092818 | ||||||
chr5:133092819
|
T | C | 3 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0073 | 3 | HG01243.hp1 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1650+30T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092819 | ||||||
chr5:133092863
|
C | A | 2 | a0001c0001t0032g0149a0001c0001t0033g0148 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1650+74C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092863 | ||||||
chr5:133092887
|
C | A | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+98C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092887 | ||||||
chr5:133092889
|
C | T | 1 | a0001c0001t0005g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1650+100C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092889 | ||||||
chr5:133092900
|
A | C | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+111A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092900 | ||||||
chr5:133092956
|
G | A | 1 | a0002c0003t0046g0152 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1650+167G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133092956 | ||||||
chr5:133092985
|
AT | A | 72 | a0001c0001t0001g0328a0001c0001t0003g0076a0001c0001t0003g0085others(69): Show | 72 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1650+212delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092985 | |||||
chr5:133092985
|
ATT | A | 59 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1650+211_1650+212d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133092985 | |||||
chr5:133093083
|
G | T | 1 | a0001c0001t0005g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1650+294G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093083 | ||||||
chr5:133093125
|
C | T | 3 | a0001c0002t0002g0050a0001c0002t0002g0069a0001c0002t0077g0026 | 3 | HG00140.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1650+336C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093125 | ||||||
chr5:133093144
|
G | C | 3 | a0001c0001t0007g0308a0001c0001t0007g0310a0001c0001t0010g0309 | 3 | NA18942.hp1 NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1650+355G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093144 | ||||||
chr5:133093166
|
A | G | 1 | a0001c0001t0065g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1650+377A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093166 | ||||||
chr5:133093173
|
A | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650+384A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093173 | ||||||
chr5:133093243
|
T | G | 1 | a0001c0001t0009g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1650+454T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093243 | ||||||
chr5:133093255
|
T | C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1650+466T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093255 | ||||||
chr5:133093571
|
G | GC | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1650+787dupC | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 133093571 | |||||
chr5:133093572
|
C | T | 1 | a0001c0001t0004g0191 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1650+783C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093572 | ||||||
chr5:133093716
|
C | G | 3 | a0001c0001t0019g0081a0001c0001t0024g0080a0001c0001t0024g0082 | 3 | HG01243.hp2 HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1650+927C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093716 | ||||||
chr5:133093806
|
G | A | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+1017G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093806 | ||||||
chr5:133093860
|
C | T | 43 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1650+1071C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093860 | ||||||
chr5:133093893
|
G | T | 1 | a0001c0002t0002g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1650+1104G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093893 | ||||||
chr5:133093921
|
C | T | 1 | a0001c0001t0024g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1650+1132C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133093921 | ||||||
chr5:133094104
|
T | A | 1 | a0001c0001t0001g0217 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1650+1315T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094104 | ||||||
chr5:133094109
|
A | G | 1 | a0001c0002t0002g0050 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1650+1320A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094109 | ||||||
chr5:133094155
|
G | A | 1 | a0001c0001t0014g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650+1366G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094155 | ||||||
chr5:133094172
|
A | C | 1 | a0001c0001t0008g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1650+1383A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094172 | ||||||
chr5:133094304
|
A | G | 1 | a0001c0001t0067g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1650+1515A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094304 | ||||||
chr5:133094462
|
G | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1651-1636G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094462 | ||||||
chr5:133094478
|
A | G | 1 | a0001c0002t0011g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1651-1620A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094478 | ||||||
chr5:133094497
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1651-1601T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094497 | ||||||
chr5:133094833
|
T | C | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0007others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1651-1265T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133094833 | ||||||
chr5:133095000
|
G | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1651-1098G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095000 | ||||||
chr5:133095157
|
A | G | 1 | a0001c0001t0017g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1651-941A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095157 | ||||||
chr5:133095288
|
C | T | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-810C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095288 | ||||||
chr5:133095309
|
C | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1651-789C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095309 | ||||||
chr5:133095310
|
A | G | 1 | a0001c0001t0035g0318 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1651-788A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095310 | ||||||
chr5:133095445
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1651-653A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095445 | ||||||
chr5:133095463
|
A | G | 73 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(70): Show | 73 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1651-635A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095463 | ||||||
chr5:133095621
|
C | T | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-477C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095621 | ||||||
chr5:133095693
|
G | A | 2 | a0001c0001t0005g0235a0001c0001t0006g0307 | 2 | NA18972.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1651-405G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133095693 | ||||||
chr5:133096034
|
A | T | 1 | a0001c0001t0063g0356 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1651-64A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 13/18 | chr5 | 133096034 | ||||||
chr5:133096306
|
A | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1803+56A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096306 | ||||||
chr5:133096383
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0225a0001c0001t0001g0251others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1803+133G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096383 | ||||||
chr5:133096430
|
C | A | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1803+180C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096430 | ||||||
chr5:133096560
|
T | G | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1803+310T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096560 | ||||||
chr5:133096825
|
T | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1804-336T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096825 | ||||||
chr5:133096826
|
G | A | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1804-335G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096826 | ||||||
chr5:133096838
|
C | T | 66 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(63): Show | 68 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1804-323C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096838 | ||||||
chr5:133096954
|
A | G | 1 | a0001c0001t0005g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1804-207A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096954 | ||||||
chr5:133096976
|
C | G | 3 | a0001c0001t0005g0233a0001c0001t0005g0237a0001c0001t0043g0214 | 3 | NA18971.hp1 NA19011.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1804-185C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 14/18 | chr5 | 133096976 | ||||||
chr5:133097357
|
G | T | 10 | a0001c0001t0009g0168a0001c0001t0009g0173a0001c0001t0012g0166others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1929+71G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097357 | ||||||
chr5:133097427
|
T | A | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1929+141T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097427 | ||||||
chr5:133097511
|
C | G | 56 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1929+225C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097511 | ||||||
chr5:133097531
|
G | A | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1929+245G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097531 | ||||||
chr5:133097535
|
CTTTCT | C | 8 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0131others(5): Show | 8 | HG01167.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1929+263_1929+267d others(7): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097535 | |||||
chr5:133097549
|
C | CT | 59 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1929+279dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097549 | |||||
chr5:133097605
|
G | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1929+319G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097605 | ||||||
chr5:133097631
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+345C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097631 | ||||||
chr5:133097815
|
C | T | 4 | a0001c0002t0002g0003a0001c0002t0002g0072a0001c0002t0002g0073others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+529C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097815 | ||||||
chr5:133097891
|
A | G | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+605A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097891 | ||||||
chr5:133097911
|
G | GT | 9 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0350others(6): Show | 9 | HG01106.hp2 HG01167.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1929+640dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133097911 | |||||
chr5:133097913
|
T | G | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1929+627T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097913 | ||||||
chr5:133097926
|
T | A | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1929+640T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097926 | ||||||
chr5:133097929
|
T | G | 1 | a0001c0002t0011g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1929+643T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133097929 | ||||||
chr5:133098036
|
C | T | 1 | a0001c0001t0059g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1929+750C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098036 | ||||||
chr5:133098334
|
C | T | 1 | a0001c0001t0042g0210 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1929+1048C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098334 | ||||||
chr5:133098350
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+1064C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098350 | ||||||
chr5:133098440
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1930-1105T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098440 | ||||||
chr5:133098467
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1930-1078A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098467 | ||||||
chr5:133098470
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0007g0336 | 2 | HG01255.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1930-1075C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098470 | ||||||
chr5:133098478
|
AT | A | 148 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(145): Show | 150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1930-1053delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133098478 | |||||
chr5:133098575
|
G | A | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1930-970G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098575 | ||||||
chr5:133098634
|
CTTTA | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-906_1930-903d others(6): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133098634 | |||||
chr5:133098638
|
A | G | 1 | a0001c0001t0004g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1930-907A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098638 | ||||||
chr5:133098719
|
C | T | 56 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1930-826C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098719 | ||||||
chr5:133098769
|
T | C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1930-776T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098769 | ||||||
chr5:133098862
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0008g0261 | 2 | NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1930-683G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098862 | ||||||
chr5:133098913
|
C | G | 2 | a0001c0002t0030g0001a0001c0002t0075g0027 | 3 | HG00323.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1930-632C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098913 | ||||||
chr5:133098916
|
G | C | 14 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0088others(11): Show | 14 | HG00438.hp1 NA18942.hp2 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.1930-629G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098916 | ||||||
chr5:133098957
|
G | C | 70 | a0001c0001t0002g0074a0001c0001t0072g0015a0001c0001t0074g0019others(67): Show | 72 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1930-588G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133098957 | ||||||
chr5:133099139
|
AT | A | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-398delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 133099139 | |||||
chr5:133099189
|
G | A | 2 | a0001c0001t0064g0018a0001c0001t0067g0017 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1930-356G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099189 | ||||||
chr5:133099190
|
C | T | 1 | a0001c0001t0007g0324 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1930-355C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099190 | ||||||
chr5:133099195
|
T | C | 1 | a0001c0001t0008g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1930-350T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099195 | ||||||
chr5:133099270
|
C | T | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-275C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099270 | ||||||
chr5:133099314
|
G | T | 1 | a0001c0001t0004g0335 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1930-231G>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099314 | ||||||
chr5:133099411
|
G | C | 20 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0008g0083others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1930-134G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099411 | ||||||
chr5:133099417
|
G | A | 3 | a0001c0001t0005g0192a0001c0001t0005g0302a0001c0001t0006g0344 | 3 | HG00639.hp1 HG01069.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1930-128G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099417 | ||||||
chr5:133099454
|
A | C | 7 | a0001c0001t0009g0168a0001c0001t0009g0173a0001c0001t0012g0166others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-91A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 15/18 | chr5 | 133099454 | ||||||
chr5:133099729
|
T | A | 6 | a0001c0001t0032g0149a0001c0001t0033g0148a0001c0001t0064g0018others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037+77T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099729 | ||||||
chr5:133099796
|
C | T | 62 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(59): Show | 64 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2037+144C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099796 | ||||||
chr5:133099880
|
C | T | 150 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(147): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2037+228C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133099880 | ||||||
chr5:133100064
|
T | C | 1 | a0001c0001t0008g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2037+412T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100064 | ||||||
chr5:133100252
|
CAG | C | 3 | a0001c0001t0025g0004a0001c0001t0025g0182a0001c0001t0051g0004 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2037+601_2037+602d others(4): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100252 | ||||||
chr5:133100261
|
T | C | 1 | a0001c0001t0004g0208 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2037+609T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100261 | ||||||
chr5:133100482
|
C | T | 2 | a0001c0001t0041g0122a0001c0001t0050g0121 | 2 | NA18953.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2037+830C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100482 | ||||||
chr5:133100527
|
C | T | 63 | a0001c0001t0002g0074a0001c0001t0074g0019a0001c0002t0002g0002others(60): Show | 65 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.2037+875C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100527 | ||||||
chr5:133100636
|
T | G | 1 | a0001c0001t0008g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2037+984T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100636 | ||||||
chr5:133100645
|
C | T | 1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2037+993C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100645 | ||||||
chr5:133100666
|
T | C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2037+1014T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100666 | ||||||
chr5:133100700
|
C | A | 154 | a0001c0001t0002g0074a0001c0001t0003g0076a0001c0001t0003g0085others(151): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.2037+1048C>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100700 | ||||||
chr5:133100799
|
T | G | 1 | a0001c0001t0010g0262 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2038-960T>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133100799 | ||||||
chr5:133101247
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2038-512C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101247 | ||||||
chr5:133101560
|
G | A | 4 | a0001c0001t0012g0084a0001c0001t0020g0140a0001c0001t0020g0144others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-199G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101560 | ||||||
chr5:133101634
|
A | T | 1 | a0001c0001t0004g0208 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2038-125A>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101634 | ||||||
chr5:133101718
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2038-41C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 16/18 | chr5 | 133101718 | ||||||
chr5:133101902
|
C | T | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2157+24C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101902 | ||||||
chr5:133101903
|
T | A | 10 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(7): Show | 10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2157+25T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101903 | ||||||
chr5:133101904
|
T | A | 10 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(7): Show | 10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2157+26T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101904 | ||||||
chr5:133101921
|
C | CT | 17 | a0001c0001t0001g0162a0001c0001t0001g0204a0001c0001t0001g0220others(14): Show | 17 | HG00280.hp1 HG01175.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2157+66dupT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | |||||
chr5:133101921
|
CT | C | 28 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0332others(25): Show | 28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2157+66delT | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | |||||
chr5:133101921
|
CTT | C | 60 | a0001c0001t0002g0074a0001c0001t0015g0171a0001c0001t0074g0019others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2157+65_2157+66del others(2): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | |||||
chr5:133101921
|
CTTT | C | 61 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(58): Show | 61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2157+64_2157+66del others(3): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | |||||
chr5:133101921
|
CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+55_2157+66del others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133101921 | |||||
chr5:133101984
|
T | C | 1 | a0001c0001t0072g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2157+106T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133101984 | ||||||
chr5:133102051
|
C | T | 1 | a0001c0001t0007g0298 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2157+173C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102051 | ||||||
chr5:133102197
|
C | T | 1 | a0001c0001t0007g0258 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2157+319C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102197 | ||||||
chr5:133102226
|
C | T | 16 | a0001c0001t0008g0130a0001c0001t0008g0132a0001c0001t0008g0133others(13): Show | 16 | HG01496.hp1 HG02109.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+348C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102226 | ||||||
chr5:133102275
|
G | C | 1 | a0001c0001t0067g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2157+397G>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102275 | ||||||
chr5:133102343
|
G | A | 57 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0001g0217others(54): Show | 57 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2157+465G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102343 | ||||||
chr5:133102372
|
A | C | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2157+494A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102372 | ||||||
chr5:133102666
|
C | T | 67 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(64): Show | 69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.2157+788C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102666 | ||||||
chr5:133102689
|
T | C | 1 | a0001c0001t0066g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2157+811T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102689 | ||||||
chr5:133102913
|
C | CTTTTTTT others(1): Show |
60 | a0001c0001t0002g0074a0001c0001t0017g0353a0001c0001t0017g0354others(57): Show | 61 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2158-942_2158-935d others(10): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102913
|
C | CTTTTTTT others(2): Show |
17 | a0001c0001t0003g0094a0001c0001t0008g0083a0001c0001t0014g0128others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2158-943_2158-935d others(11): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102913
|
C | CTTTTTTT others(3): Show |
88 | a0001c0001t0001g0162a0001c0001t0003g0085a0001c0001t0003g0086others(85): Show | 88 | HG00438.hp1 HG00558.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.2158-944_2158-935d others(12): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102913
|
C | CTTTTTTT others(4): Show |
13 | a0001c0001t0001g0160a0001c0001t0003g0076a0001c0001t0003g0092others(10): Show | 13 | HG00609.hp2 HG01106.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2158-945_2158-935d others(13): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102913
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0019g0081a0001c0001t0057g0104 | 2 | HG03041.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2158-946_2158-935d others(14): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102913
|
C | CTTTTTTT others(15): Show |
1 | a0010c0008t0073g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2158-935_2158-934i others(24): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 133102913 | |||||
chr5:133102993
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C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | NA18974.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2158-872C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102993 | ||||||
chr5:133102996
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C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0225a0001c0001t0001g0251others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.2158-869C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133102996 | ||||||
chr5:133103008
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A | G | 6 | a0001c0001t0082g0014a0001c0004t0021g0009a0001c0004t0021g0011others(3): Show | 6 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2158-857A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103008 | ||||||
chr5:133103063
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T | C | 3 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2158-802T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103063 | ||||||
chr5:133103070
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T | C | 7 | a0001c0001t0072g0015a0001c0001t0082g0014a0001c0004t0021g0009others(4): Show | 7 | HG02055.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158-795T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103070 | ||||||
chr5:133103167
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C | T | 1 | a0001c0001t0001g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2158-698C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103167 | ||||||
chr5:133103267
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T | C | 56 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2158-598T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103267 | ||||||
chr5:133103278
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A | C | 56 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2158-587A>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103278 | ||||||
chr5:133103318
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T | A | 74 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(71): Show | 76 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2158-547T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103318 | ||||||
chr5:133103318
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T | C | 3 | a0001c0001t0013g0266a0001c0001t0028g0256a0001c0001t0028g0257 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2158-547T>C | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103318 | ||||||
chr5:133103336
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C | T | 67 | a0001c0001t0002g0074a0001c0001t0017g0352a0001c0001t0017g0353others(64): Show | 69 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.2158-529C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103336 | ||||||
chr5:133103403
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C | T | 1 | a0001c0001t0015g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2158-462C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103403 | ||||||
chr5:133103437
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C | G | 1 | a0001c0001t0012g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2158-428C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103437 | ||||||
chr5:133103454
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C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0219a0001c0001t0005g0295 | 3 | NA18747.hp2 NA18970.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2158-411C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103454 | ||||||
chr5:133103470
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G | A | 1 | a0003c0005t0009g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2158-395G>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103470 | ||||||
chr5:133103682
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C | T | 1 | a0001c0002t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2158-183C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103682 | ||||||
chr5:133103810
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C | T | 1 | a0001c0001t0006g0250 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2158-55C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | chr5 | 133103810 | ||||||
chr5:133104046
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T | A | 4 | a0001c0001t0017g0352a0001c0001t0017g0353a0001c0001t0017g0354others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+20T>A | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104046 | ||||||
chr5:133104063
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C | T | 1 | a0001c0001t0010g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2319+37C>T | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104063 | ||||||
chr5:133104115
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A | G | 2 | a0001c0001t0001g0274a0001c0001t0007g0339 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2319+89A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104115 | ||||||
chr5:133104128
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C | G | 56 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0086others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2319+102C>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104128 | ||||||
chr5:133104139
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A | G | 1 | a0001c0001t0008g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2320-94A>G | HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 18/18 | chr5 | 133104139 |