Variant report

Variant	rs3922472
Chromosome Location	chr2:181772262-181772263
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:181770939..181772876-chr2:181773303..181775237,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-2	chr2:181771313-181774666	NONHSAT075852

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10178270	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10189224	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11894079	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12328545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12471143	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3922471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4128869	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs4128870	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4290619	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4315481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4359601	0.98[ASN][1000 genomes]
rs4422130	0.81[EUR][1000 genomes]
rs4436925	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4666643	0.93[ASN][1000 genomes]
rs4666946	0.95[ASN][1000 genomes]
rs4666957	0.98[ASN][1000 genomes]
rs62178161	0.81[EUR][1000 genomes]
rs62178173	0.81[EUR][1000 genomes]
rs62178176	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62178210	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62178239	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62178240	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6724902	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6730421	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6756832	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9677524	0.89[ASN][1000 genomes]
rs9677649	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875476	chr2:181767757-181854997	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181770600-181772400	Weak transcription	HSMM	muscle
2	chr2:181770800-181772400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:181770800-181775400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr2:181771000-181772600	Weak transcription	Fetal Lung	lung
5	chr2:181771800-181772800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:181772000-181773400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:181772000-181773600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:181772000-181775600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:181772200-181773200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:181772200-181773200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:181772200-181773200	Enhancers	NHDF-Ad	bronchial
12	chr2:181772200-181773200	Enhancers	Osteobl	bone

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