Variant report

Variant	rs11695218
Chromosome Location	chr2:124942819-124942820
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10496634	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11679836	0.84[EUR][1000 genomes]
rs11682281	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11682449	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1170619	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1170621	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1184930	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11891838	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11899935	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11902121	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12473278	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12473309	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12987836	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1529298	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1529299	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17011004	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17011031	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17011040	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17011058	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35122611	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4848919	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56321724	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56369586	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs57578864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62163932	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62163933	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62163934	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs749196	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7561523	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7561939	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7584334	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7598484	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:124938600-124943200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:124938600-124943200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:124938600-124954400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:124942800-124945800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:124942800-124947200	Enhancers	HUES64 Cell Line	embryonic stem cell

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