Variant report

Variant	rs72836304
Chromosome Location	chr2:111773532-111773533
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:111772315..111773850-chr2:111797935..111799748,2	MCF-7	breast:
2	chr2:111772841..111774627-chr2:111779212..111780860,2	MCF-7	breast:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13339827	0.84[ASN][1000 genomes]
rs1384791	0.85[ASN][1000 genomes]
rs1384794	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs55833189	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56105404	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs59486976	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs61145952	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs66509834	0.85[ASN][1000 genomes]
rs67234811	0.80[ASN][1000 genomes]
rs67250604	0.85[ASN][1000 genomes]
rs6730256	0.89[ASN][1000 genomes]
rs68080118	0.87[ASN][1000 genomes]
rs72834562	0.80[ASN][1000 genomes]
rs72834571	0.80[ASN][1000 genomes]
rs72834576	0.85[ASN][1000 genomes]
rs72834578	0.85[ASN][1000 genomes]
rs72834584	0.85[ASN][1000 genomes]
rs72834594	0.87[ASN][1000 genomes]
rs72834595	0.87[ASN][1000 genomes]
rs72836353	1.00[AFR][1000 genomes]
rs72946240	0.87[ASN][1000 genomes]
rs7420839	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997829	chr2:111486961-111780537	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv834330	chr2:111593290-111789447	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1004949	chr2:111607532-111780719	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1002568	chr2:111607532-111781442	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111770200-111786600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:111772000-111773600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr2:111772200-111777200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr2:111772400-111774400	Enhancers	Fetal Brain Male	brain
5	chr2:111772800-111780200	Enhancers	Primary monocytes fromperipheralblood	blood

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