Variant report
Variant | rs57494426 |
---|---|
Chromosome Location | chr11:85132393-85132394 |
allele | C/T |
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 | 0.94[ASN][1000 genomes] |
rs10501592 | 0.80[EUR][1000 genomes] |
rs11827749 | 0.91[ASN][1000 genomes] |
rs12788992 | 0.81[EUR][1000 genomes] |
rs1509812 | 1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs17148063 | 0.84[EUR][1000 genomes] |
rs17148067 | 0.81[EUR][1000 genomes] |
rs17148070 | 0.81[EUR][1000 genomes] |
rs17148078 | 0.81[EUR][1000 genomes] |
rs17208108 | 0.81[EUR][1000 genomes] |
rs17208150 | 0.84[EUR][1000 genomes] |
rs17208171 | 0.81[EUR][1000 genomes] |
rs17208192 | 0.81[EUR][1000 genomes] |
rs17810357 | 0.81[EUR][1000 genomes] |
rs17810405 | 0.84[EUR][1000 genomes] |
rs17810429 | 0.81[EUR][1000 genomes] |
rs17810490 | 0.88[EUR][1000 genomes] |
rs17810611 | 1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1812352 | 0.91[ASN][1000 genomes] |
rs1914372 | 0.84[EUR][1000 genomes] |
rs2036782 | 0.87[ASN][1000 genomes] |
rs2213116 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs57104960 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs58117031 | 1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs58464081 | 0.84[EUR][1000 genomes] |
rs58649506 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs59015145 | 0.89[ASN][1000 genomes] |
rs59464672 | 1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs59713586 | 0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs59869002 | 0.81[ASN][1000 genomes] |
rs60284674 | 0.84[EUR][1000 genomes] |
rs60360244 | 0.84[EUR][1000 genomes] |
rs61697848 | 0.84[EUR][1000 genomes] |
rs7117010 | 0.87[ASN][1000 genomes] |
rs72947971 | 0.81[EUR][1000 genomes] |
rs72947974 | 0.84[EUR][1000 genomes] |
rs72947975 | 0.84[EUR][1000 genomes] |
rs72947981 | 0.84[EUR][1000 genomes] |
rs72947999 | 0.81[EUR][1000 genomes] |
rs72950107 | 0.84[EUR][1000 genomes] |
rs72950128 | 0.81[EUR][1000 genomes] |
rs72950129 | 0.81[EUR][1000 genomes] |
rs72950131 | 0.81[EUR][1000 genomes] |
rs72950141 | 0.84[EUR][1000 genomes] |
rs72950152 | 0.84[EUR][1000 genomes] |
rs72950153 | 0.84[EUR][1000 genomes] |
rs72950156 | 0.81[EUR][1000 genomes] |
rs72950157 | 0.81[EUR][1000 genomes] |
rs72950158 | 0.81[EUR][1000 genomes] |
rs72950161 | 0.81[EUR][1000 genomes] |
rs72950165 | 0.85[EUR][1000 genomes] |
rs72950167 | 0.88[EUR][1000 genomes] |
rs72950168 | 0.81[EUR][1000 genomes] |
rs72950169 | 0.88[EUR][1000 genomes] |
rs72950175 | 0.88[EUR][1000 genomes] |
rs72950176 | 0.88[EUR][1000 genomes] |
rs72950181 | 0.88[EUR][1000 genomes] |
rs72950182 | 0.88[EUR][1000 genomes] |
rs72950186 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72951917 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72951920 | 1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs72951948 | 0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs72951958 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72951961 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72951976 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72951982 | 1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs72951984 | 1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs72951987 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72951995 | 0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72952002 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72953904 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72953907 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72953908 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72953913 | 0.92[EUR][1000 genomes] |
rs72953914 | 0.92[EUR][1000 genomes] |
rs72953916 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72953921 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72953926 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72953932 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72953934 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72953938 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7947098 | 0.92[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 |
7 | nsv1035905 | chr11:85130543-85220773 | Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:85132200-85132800 | ZNF genes & repeats | Skeletal Muscle Female | skeletal muscle |