Variant report

Variant	rs10178270
Chromosome Location	chr2:181773395-181773396
allele	C/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]
rs10189224	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11894079	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12328545	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12471143	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3922471	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3922472	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4128869	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4128870	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4290619	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4315481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4359601	1.00[ASN][1000 genomes]
rs4422130	0.81[EUR][1000 genomes]
rs4436925	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4666643	0.95[ASN][1000 genomes]
rs4666946	0.97[ASN][1000 genomes]
rs4666957	1.00[ASN][1000 genomes]
rs62178161	0.81[EUR][1000 genomes]
rs62178173	0.81[EUR][1000 genomes]
rs62178176	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62178210	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62178239	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62178240	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6724902	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6730421	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6756832	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9677524	0.91[ASN][1000 genomes]
rs9677649	0.90[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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181770800-181775400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:181772000-181773400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:181772000-181773600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:181772000-181775600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:181772600-181773600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:181772600-181774000	Enhancers	A549	lung
7	chr2:181773000-181773600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:181773200-181775800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:181773200-181776000	Weak transcription	Osteobl	bone

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