Variant report
Variant | rs57106172 |
---|---|
Chromosome Location | chr11:93706141-93706142 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10501813 | 0.94[ASN][1000 genomes] |
rs11825709 | 1.00[ASN][1000 genomes] |
rs1401184 | 0.94[ASN][1000 genomes] |
rs1518560 | 0.90[ASN][1000 genomes] |
rs1589166 | 0.94[ASN][1000 genomes] |
rs1607401 | 0.94[ASN][1000 genomes] |
rs1850656 | 0.89[ASN][1000 genomes] |
rs1894165 | 0.94[ASN][1000 genomes] |
rs1894166 | 0.91[ASN][1000 genomes] |
rs1945786 | 0.90[ASN][1000 genomes] |
rs1945787 | 0.90[ASN][1000 genomes] |
rs2020351 | 0.90[ASN][1000 genomes] |
rs2102857 | 0.94[ASN][1000 genomes] |
rs2139089 | 0.90[ASN][1000 genomes] |
rs2176563 | 0.94[ASN][1000 genomes] |
rs2203793 | 0.94[ASN][1000 genomes] |
rs2213108 | 0.89[ASN][1000 genomes] |
rs2213110 | 0.92[ASN][1000 genomes] |
rs2399750 | 0.90[ASN][1000 genomes] |
rs2460049 | 0.83[ASN][1000 genomes] |
rs2460050 | 0.90[ASN][1000 genomes] |
rs2460052 | 0.88[ASN][1000 genomes] |
rs2460053 | 0.94[ASN][1000 genomes] |
rs2460064 | 0.91[ASN][1000 genomes] |
rs2460065 | 0.94[ASN][1000 genomes] |
rs2460069 | 0.90[ASN][1000 genomes] |
rs2460070 | 0.94[ASN][1000 genomes] |
rs2462733 | 0.94[ASN][1000 genomes] |
rs2462735 | 0.94[ASN][1000 genomes] |
rs2462756 | 0.93[ASN][1000 genomes] |
rs2462757 | 0.88[ASN][1000 genomes] |
rs2462758 | 0.94[ASN][1000 genomes] |
rs2462759 | 0.90[ASN][1000 genomes] |
rs2462760 | 0.92[ASN][1000 genomes] |
rs2462763 | 0.90[ASN][1000 genomes] |
rs2511380 | 0.90[ASN][1000 genomes] |
rs2511381 | 0.84[ASN][1000 genomes] |
rs2511403 | 0.88[ASN][1000 genomes] |
rs2511411 | 0.94[ASN][1000 genomes] |
rs56938392 | 0.96[ASN][1000 genomes] |
rs57586533 | 1.00[ASN][1000 genomes] |
rs57953549 | 0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs59689949 | 1.00[ASN][1000 genomes] |
rs59793398 | 0.96[ASN][1000 genomes] |
rs66480929 | 0.84[ASN][1000 genomes] |
rs66514329 | 0.94[ASN][1000 genomes] |
rs66523751 | 0.88[ASN][1000 genomes] |
rs66538341 | 0.89[ASN][1000 genomes] |
rs66918645 | 0.84[ASN][1000 genomes] |
rs66977226 | 1.00[ASN][1000 genomes] |
rs67001808 | 0.96[ASN][1000 genomes] |
rs67243356 | 0.89[ASN][1000 genomes] |
rs67412659 | 0.96[ASN][1000 genomes] |
rs67988338 | 1.00[ASN][1000 genomes] |
rs72964631 | 0.96[ASN][1000 genomes] |
rs72964645 | 0.96[ASN][1000 genomes] |
rs72964666 | 0.94[ASN][1000 genomes] |
rs73551180 | 0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs73564796 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73564799 | 0.96[ASN][1000 genomes] |
rs959342 | 0.91[ASN][1000 genomes] |
rs959343 | 0.91[ASN][1000 genomes] |
rs978777 | 0.93[ASN][1000 genomes] |
rs9787791 | 0.84[ASN][1000 genomes] |
rs989088 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv508650 | chr11:93609010-93713576 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1049467 | chr11:93651025-93778717 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv442 | chr11:93665117-93717973 | Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | esv2757466 | chr11:93676224-93714950 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv2759854 | chr11:93676224-93714950 | Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:93705800-93706400 | Enhancers | K562 | blood |
2 | chr11:93705800-93707200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |