Variant report

Variant	rs11225392
Chromosome Location	chr11:102579764-102579765
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:102579717-102579776	GM13976	blood:	n/a	n/a

Variant related genes	Relation type
MMP27	TF binding region

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12099177	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17093633	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17099411	0.84[AMR][1000 genomes]
rs17099419	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17099436	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17099451	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17099452	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1892885	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1940052	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2508383	0.83[ASN][1000 genomes]
rs34433762	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35308160	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35800658	0.94[AFR][1000 genomes]
rs3740936	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3740938	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3758860	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4376870	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4498962	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4564300	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4754049	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4754866	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754867	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754869	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754870	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4754871	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4754872	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4754874	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4754876	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58406046	0.84[AMR][1000 genomes]
rs60059188	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs60964518	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72973547	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72973559	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72973562	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72973563	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72975539	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72975567	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102572600-102579800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:102577000-102579800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:102577000-102579800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:102577200-102580200	Weak transcription	NHDF-Ad	bronchial
5	chr11:102579600-102581200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:102579600-102581600	Enhancers	Monocytes-CD14+_RO01746	blood

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