Variant report

Variant	rs2602484
Chromosome Location	chr11:77011783-77011784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10793243	0.82[AFR][1000 genomes]
rs10899366	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10899367	0.94[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs11237200	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs11820118	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs11823572	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11828786	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs12420360	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs1670445	0.82[ASN][1000 genomes]
rs1670455	0.81[ASN][1000 genomes]
rs1893756	0.86[EUR][1000 genomes]
rs1893757	0.86[EUR][1000 genomes]
rs1944033	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2100393	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2156862	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2156863	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.81[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2276289	0.86[EUR][1000 genomes]
rs2282576	1.00[CEU][hapmap]
rs2602471	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2602473	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs2602474	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2602475	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2602480	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2602481	1.00[CHB][hapmap];0.87[JPT][hapmap];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2602482	1.00[CHB][hapmap];0.87[JPT][hapmap];0.92[ASN][1000 genomes]
rs2725829	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2729756	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs2729758	0.95[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs2729763	0.83[ASN][1000 genomes]
rs2729772	1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2729775	0.88[CHB][hapmap]
rs2844327	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs2852388	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2852390	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs2853085	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs2853094	0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2853095	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs2853098	0.95[CHB][hapmap]
rs2888377	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs34375485	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3740769	1.00[YRI][hapmap]
rs4944151	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs4944156	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4945161	0.87[JPT][hapmap]
rs7125798	0.81[YRI][hapmap]
rs733358	0.89[CHB][hapmap];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs876319	0.95[CHB][hapmap];0.82[JPT][hapmap]
rs947810	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs948959	1.00[CEU][hapmap];0.95[YRI][hapmap]
rs9634030	0.95[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534515	chr11:76900813-77035769	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv3424135	chr11:76961603-77277087	Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77004400-77012600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:77010200-77012400	Enhancers	HepG2	liver
3	chr11:77010200-77012600	Enhancers	Stomach Mucosa	stomach
4	chr11:77011000-77012600	Enhancers	A549	lung

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