Variant report

Variant	rs7324463
Chromosome Location	chr13:93060780-93060781
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	chr13:93058377..93060985-chr13:93069058..93071166,2	K562	blood:
2	chr13:93057853..93060385-chr13:93060561..93063172,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1023013	0.82[CHB][hapmap];0.97[CHD][hapmap];0.91[ASN][1000 genomes]
rs1023014	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1116887	0.84[JPT][hapmap]
rs1926608	0.91[ASN][1000 genomes]
rs1926609	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1926610	0.86[CHB][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2094475	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs2104624	0.82[CHB][hapmap]
rs2209836	0.82[CHB][hapmap];0.89[ASN][1000 genomes]
rs2209839	0.82[CHB][hapmap]
rs2209840	0.82[CHB][hapmap]
rs2225158	0.82[CHB][hapmap];0.97[CHD][hapmap];0.88[ASN][1000 genomes]
rs2374006	0.90[ASN][1000 genomes]
rs2888720	0.85[CHD][hapmap]
rs4142024	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4771859	0.82[CHB][hapmap];0.97[CHD][hapmap]
rs4773682	0.82[CHB][hapmap];0.88[ASN][1000 genomes]
rs6492607	0.82[CHB][hapmap];0.97[CHD][hapmap]
rs7317952	0.88[ASN][1000 genomes]
rs7318720	0.92[CEU][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes]
rs7329163	0.80[TSI][hapmap]
rs7329553	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs7988626	0.89[ASN][1000 genomes]
rs7996390	0.82[CHB][hapmap];0.88[ASN][1000 genomes]
rs927966	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs9301803	0.82[TSI][hapmap]
rs9516072	0.82[CHB][hapmap];0.97[CHD][hapmap];0.88[ASN][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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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