Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:133406880-133407030	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:133399204..133402131-chr6:133405964..133408211,2	MCF-7	breast:

Variant related genes	Relation type
LINC00326	TF binding region

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11963825	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11965251	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11965334	0.91[ASN][1000 genomes]
rs11966375	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs11968671	0.85[ASN][1000 genomes]
rs34704641	0.85[ASN][1000 genomes]
rs4076846	0.95[ASN][1000 genomes]
rs4458711	0.95[ASN][1000 genomes]
rs4569980	0.95[ASN][1000 genomes]
rs5010276	1.00[ASN][1000 genomes]
rs5020765	0.95[ASN][1000 genomes]
rs56026451	1.00[ASN][1000 genomes]
rs56235131	1.00[ASN][1000 genomes]
rs57161904	1.00[ASN][1000 genomes]
rs57261444	1.00[ASN][1000 genomes]
rs57940911	0.95[ASN][1000 genomes]
rs58175086	0.95[ASN][1000 genomes]
rs58190426	1.00[ASN][1000 genomes]
rs58336680	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58519358	1.00[ASN][1000 genomes]
rs59430285	1.00[ASN][1000 genomes]
rs60000557	1.00[ASN][1000 genomes]
rs60082145	1.00[ASN][1000 genomes]
rs60484160	1.00[ASN][1000 genomes]
rs60576607	1.00[ASN][1000 genomes]
rs60622734	1.00[ASN][1000 genomes]
rs60804293	1.00[ASN][1000 genomes]
rs61006452	0.95[ASN][1000 genomes]
rs61244591	1.00[ASN][1000 genomes]
rs61362264	1.00[ASN][1000 genomes]
rs61555922	1.00[ASN][1000 genomes]
rs73553617	1.00[ASN][1000 genomes]
rs73773507	0.95[ASN][1000 genomes]
rs73773508	0.95[ASN][1000 genomes]
rs73773509	0.95[ASN][1000 genomes]
rs73773520	0.91[ASN][1000 genomes]
rs73773521	0.91[ASN][1000 genomes]
rs73773523	1.00[ASN][1000 genomes]
rs7747170	1.00[ASN][1000 genomes]
rs9493507	1.00[TSI][hapmap]

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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv428154	chr6:133271975-133522803	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3445931	chr6:133347824-133434532	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv519475	chr6:133350936-133474673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 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	chr6:133403000-133407200	Weak transcription	Fetal Lung	lung
2	chr6:133405000-133407200	Weak transcription	Psoas Muscle	Psoas
3	chr6:133406400-133407200	Weak transcription	Fetal Muscle Leg	muscle

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