Variant report

Variant	rs10931344
Chromosome Location	chr2:189106677-189106678
allele	C/T
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: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10175259	0.87[ASN][1000 genomes]
rs10180222	0.89[ASN][1000 genomes]
rs1036649	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10804020	0.87[JPT][hapmap];0.80[YRI][hapmap]
rs10931343	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11900558	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12464904	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs12465164	0.80[JPT][hapmap]
rs12465625	0.80[JPT][hapmap]
rs12613615	0.83[ASN][1000 genomes]
rs12619361	0.89[ASN][1000 genomes]
rs12624002	0.80[JPT][hapmap]
rs12693487	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12693489	0.83[ASN][1000 genomes]
rs13008931	0.85[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap];0.82[ASN][1000 genomes]
rs1898986	0.97[ASN][1000 genomes]
rs4132426	0.81[EUR][1000 genomes]
rs4402719	0.85[ASN][1000 genomes]
rs4426503	0.82[ASN][1000 genomes]
rs4500907	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4516391	0.85[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs4591312	0.82[ASN][1000 genomes]
rs4610010	0.82[ASN][1000 genomes]
rs4641903	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4667215	0.82[ASN][1000 genomes]
rs59443840	0.87[EUR][1000 genomes]
rs6434269	0.90[CHB][hapmap];0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs6711822	0.97[ASN][1000 genomes]
rs6712056	0.82[ASN][1000 genomes]
rs6719273	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6744150	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6744629	0.85[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap];0.82[ASN][1000 genomes]
rs7425596	0.82[ASN][1000 genomes]
rs7566619	0.87[JPT][hapmap];0.81[YRI][hapmap]
rs7574262	0.87[JPT][hapmap]
rs7585703	0.90[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs7586390	0.86[JPT][hapmap];0.81[YRI][hapmap]
rs7593546	0.85[CHB][hapmap];0.87[JPT][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]
rs7598279	0.86[ASN][1000 genomes]
rs7598785	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7599516	0.85[ASN][1000 genomes]
rs893745	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]

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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189100400-189121200	Weak transcription	K562	blood

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