Variant report

Variant	rs34477786
Chromosome Location	chr2:189108567-189108568
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	chr2:189066882..189068892-chr2:189106481..189108837,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10221554	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10931351	0.80[ASN][1000 genomes]
rs11676580	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12151472	0.80[ASN][1000 genomes]
rs12151502	0.80[ASN][1000 genomes]
rs12151631	0.80[ASN][1000 genomes]
rs12614592	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13389609	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13403138	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13416775	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13432874	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829913	0.98[ASN][1000 genomes]
rs16829916	0.98[ASN][1000 genomes]
rs4337443	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4371324	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4372844	0.98[ASN][1000 genomes]
rs4453654	0.82[ASN][1000 genomes]
rs4490147	0.84[ASN][1000 genomes]
rs4536617	0.98[ASN][1000 genomes]
rs4541223	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4552156	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4595930	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60688387	0.85[ASN][1000 genomes]
rs66579041	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66725342	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6707721	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6708455	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67324207	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6735839	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6749420	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6749586	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68056256	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72901564	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72901581	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72903517	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72903530	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72907635	0.82[ASN][1000 genomes]
rs73034491	0.80[ASN][1000 genomes]
rs73034500	0.80[ASN][1000 genomes]
rs73034501	0.80[ASN][1000 genomes]
rs73036412	0.80[ASN][1000 genomes]
rs73039927	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73039929	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73041656	0.92[ASN][1000 genomes]
rs73043732	0.97[ASN][1000 genomes]
rs7559554	0.82[ASN][1000 genomes]
rs7562160	0.82[ASN][1000 genomes]
rs7577265	0.82[ASN][1000 genomes]
rs7586536	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7596399	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7601023	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9653312	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980065	0.97[EUR][1000 genomes];1.00[ASN][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	nsv1010394	chr2:188994398-189284092	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	nsv998395	chr2:189018246-189284092	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv431879	chr2:189079494-189118494	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:189100400-189121200	Weak transcription	K562	blood
2	chr2:189108200-189108600	Enhancers	Placenta	Placenta
3	chr2:189108400-189110000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:189108400-189110600	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links