Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:119907945..119910729-chr11:119942649..119945284,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10431043	0.93[ASN][1000 genomes]
rs10892514	0.90[ASN][1000 genomes]
rs10892519	0.97[ASN][1000 genomes]
rs10892521	0.96[ASN][1000 genomes]
rs11217630	0.85[ASN][1000 genomes]
rs11217633	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11217635	0.89[ASN][1000 genomes]
rs11217636	0.90[ASN][1000 genomes]
rs11217637	0.90[ASN][1000 genomes]
rs11217647	0.96[ASN][1000 genomes]
rs11217665	0.92[ASN][1000 genomes]
rs11217666	0.92[ASN][1000 genomes]
rs12223988	0.90[ASN][1000 genomes]
rs12225953	0.92[ASN][1000 genomes]
rs12573999	0.97[ASN][1000 genomes]
rs12574203	0.92[ASN][1000 genomes]
rs56745971	0.90[ASN][1000 genomes]
rs56778655	0.91[ASN][1000 genomes]
rs57510602	0.89[ASN][1000 genomes]
rs57589469	0.97[ASN][1000 genomes]
rs58844530	0.93[ASN][1000 genomes]
rs60270569	0.84[ASN][1000 genomes]
rs60914924	0.84[ASN][1000 genomes]
rs60967975	0.91[ASN][1000 genomes]
rs61218458	0.84[ASN][1000 genomes]
rs61602379	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv832285	chr11:119789595-119957724	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv508657	chr11:119891578-119971212	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119907000-119914400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr11:119908800-119910200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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