Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:18253249..18254941-chr11:18255913..18258803,2	K562	blood:

Variant related genes	Relation type
ENSG00000148965	Chromatin interaction

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10766463	0.86[EUR][1000 genomes]
rs10832908	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11024561	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11024563	0.84[EUR][1000 genomes]
rs11024578	0.87[EUR][1000 genomes]
rs2168363	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2445175	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2445176	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2445225	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2445226	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2460831	0.86[EUR][1000 genomes]
rs2468779	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2468790	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2468856	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2925145	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4757628	0.86[EUR][1000 genomes]
rs4757629	0.86[EUR][1000 genomes]
rs4757630	0.86[EUR][1000 genomes]
rs56310011	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67006796	0.86[EUR][1000 genomes]
rs67712345	0.86[EUR][1000 genomes]
rs7103794	0.86[EUR][1000 genomes]
rs7117484	0.86[EUR][1000 genomes]
rs7117890	0.86[EUR][1000 genomes]
rs7935726	0.86[EUR][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	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv428569	chr11:18194030-18350869	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18250400-18257000	Enhancers	HepG2	liver
2	chr11:18252200-18255600	Genic enhancers	Liver	Liver
3	chr11:18253400-18253600	Enhancers	Primary B cells from cord blood	blood

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