Variant report
Variant | rs7117010 |
---|---|
Chromosome Location | chr11:85097310-85097311 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1000799 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10501592 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs11821513 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11822362 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11823732 | 1.00[ASW][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs11823978 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11825901 | 0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11827372 | 1.00[ASW][hapmap];1.00[CHB][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.87[ASN][1000 genomes] |
rs11827749 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12281150 | 0.83[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap] |
rs12788992 | 0.93[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs17148044 | 1.00[JPT][hapmap] |
rs17148047 | 0.83[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap] |
rs17148049 | 0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs17148061 | 1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs17148063 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17148067 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17148070 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17148078 | 0.93[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs17148086 | 0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17148090 | 0.82[ASN][1000 genomes] |
rs17159864 | 0.82[ASN][1000 genomes] |
rs17207843 | 0.82[ASN][1000 genomes] |
rs17207864 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17208108 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17208150 | 0.91[JPT][hapmap] |
rs17208171 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17208192 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17810172 | 0.83[CHD][hapmap];0.93[JPT][hapmap] |
rs17810280 | 0.92[JPT][hapmap] |
rs17810291 | 1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs17810357 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17810405 | 0.83[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17810429 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17810490 | 0.82[ASN][1000 genomes] |
rs17810611 | 0.94[ASN][1000 genomes] |
rs1812352 | 0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1876872 | 0.91[EUR][1000 genomes] |
rs1912266 | 0.91[EUR][1000 genomes] |
rs1914371 | 1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs1914372 | 1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs2032410 | 0.83[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.86[ASN][1000 genomes] |
rs2036782 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2056182 | 1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs2213116 | 0.84[ASN][1000 genomes] |
rs57104960 | 0.84[ASN][1000 genomes] |
rs57494426 | 0.87[ASN][1000 genomes] |
rs58117031 | 0.94[ASN][1000 genomes] |
rs58464081 | 0.82[ASN][1000 genomes] |
rs58649506 | 0.84[ASN][1000 genomes] |
rs58756447 | 0.86[ASN][1000 genomes] |
rs59015145 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs59464672 | 0.94[ASN][1000 genomes] |
rs59583891 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs59713586 | 0.94[ASN][1000 genomes] |
rs59869002 | 0.84[ASN][1000 genomes] |
rs60360244 | 0.80[ASN][1000 genomes] |
rs6592235 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes] |
rs6592236 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes] |
rs7108893 | 1.00[JPT][hapmap] |
rs7112335 | 0.83[CHD][hapmap];1.00[JPT][hapmap] |
rs7129666 | 0.83[CHD][hapmap];1.00[JPT][hapmap] |
rs72945920 | 0.84[ASN][1000 genomes] |
rs72945921 | 0.84[ASN][1000 genomes] |
rs72945944 | 0.80[ASN][1000 genomes] |
rs72945948 | 0.80[ASN][1000 genomes] |
rs72945956 | 0.86[ASN][1000 genomes] |
rs72945965 | 0.86[ASN][1000 genomes] |
rs72947961 | 0.86[ASN][1000 genomes] |
rs72947963 | 0.86[ASN][1000 genomes] |
rs72947971 | 0.80[ASN][1000 genomes] |
rs72947974 | 0.80[ASN][1000 genomes] |
rs72947975 | 0.80[ASN][1000 genomes] |
rs72947981 | 0.80[ASN][1000 genomes] |
rs72947999 | 0.80[ASN][1000 genomes] |
rs72950104 | 0.86[ASN][1000 genomes] |
rs72950107 | 0.82[ASN][1000 genomes] |
rs72950109 | 0.87[ASN][1000 genomes] |
rs72950128 | 0.82[ASN][1000 genomes] |
rs72950129 | 0.82[ASN][1000 genomes] |
rs72950131 | 0.82[ASN][1000 genomes] |
rs72950137 | 0.87[ASN][1000 genomes] |
rs72950141 | 0.80[ASN][1000 genomes] |
rs72950152 | 0.82[ASN][1000 genomes] |
rs72950153 | 0.82[ASN][1000 genomes] |
rs72950156 | 0.82[ASN][1000 genomes] |
rs72950157 | 0.82[ASN][1000 genomes] |
rs72950158 | 0.82[ASN][1000 genomes] |
rs72950161 | 0.82[ASN][1000 genomes] |
rs72950165 | 0.82[ASN][1000 genomes] |
rs72950167 | 0.82[ASN][1000 genomes] |
rs72950168 | 0.82[ASN][1000 genomes] |
rs72950169 | 0.82[ASN][1000 genomes] |
rs72950175 | 0.82[ASN][1000 genomes] |
rs72950176 | 0.82[ASN][1000 genomes] |
rs72950181 | 0.82[ASN][1000 genomes] |
rs72950182 | 0.82[ASN][1000 genomes] |
rs72950186 | 0.84[ASN][1000 genomes] |
rs72951917 | 0.84[ASN][1000 genomes] |
rs72951920 | 0.94[ASN][1000 genomes] |
rs72951948 | 0.91[ASN][1000 genomes] |
rs72951958 | 0.87[ASN][1000 genomes] |
rs72951961 | 0.87[ASN][1000 genomes] |
rs72951976 | 0.81[ASN][1000 genomes] |
rs72951987 | 0.84[ASN][1000 genomes] |
rs72951995 | 0.84[ASN][1000 genomes] |
rs72952002 | 0.84[ASN][1000 genomes] |
rs72953904 | 0.84[ASN][1000 genomes] |
rs72953907 | 0.84[ASN][1000 genomes] |
rs72953908 | 0.84[ASN][1000 genomes] |
rs72953925 | 0.91[EUR][1000 genomes] |
rs7924587 | 0.87[ASN][1000 genomes] |
rs7938874 | 0.91[EUR][1000 genomes] |
rs7940610 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7947098 | 0.82[ASN][1000 genomes] |
rs7951307 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1044370 | chr11:84748993-85293233 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
2 | nsv898043 | chr11:84895033-85148689 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv898044 | chr11:84895033-85220773 | ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
4 | nsv1051155 | chr11:85006564-85721261 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
5 | nsv541110 | chr11:85006564-85721261 | Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
6 | nsv898045 | chr11:85094601-85168570 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:85096000-85099000 | Weak transcription | Fetal Muscle Leg | muscle |
2 | chr11:85096200-85097400 | Enhancers | HSMM | muscle |
3 | chr11:85096200-85097600 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
4 | chr11:85096200-85097600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
5 | chr11:85096400-85097800 | Enhancers | HUES48 Cell Line | embryonic stem cell |
6 | chr11:85096400-85097800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
7 | chr11:85096600-85097400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
8 | chr11:85096600-85097400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
9 | chr11:85096600-85097400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
10 | chr11:85096800-85097400 | Enhancers | HSMMtube | muscle |