Variant report

Variant	rs11968671
Chromosome Location	chr6:133408164-133408165
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr6:133408153-133408257	Hela-S3	cervix:	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

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11963825	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11965251	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11965334	1.00[AMR][1000 genomes]
rs34704641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4076846	0.81[ASN][1000 genomes]
rs4458711	0.81[ASN][1000 genomes]
rs4569980	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs5010276	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs5020765	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs56026451	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56235131	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57161904	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57261444	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57940911	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs58175086	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs58190426	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58336680	0.81[ASN][1000 genomes]
rs58519358	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs59430285	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60000557	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60082145	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60484160	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60576607	0.85[ASN][1000 genomes]
rs60622734	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs60804293	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61006452	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61244591	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61362264	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61555922	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73553617	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73773507	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73773508	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73773509	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73773523	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7747170	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9493506	0.85[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	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:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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