Variant report

Variant	rs11951180
Chromosome Location	chr5:114405806-114405807
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:114234220..114234829-chr5:114405733..114406270,2	MCF-7	breast:
2	chr5:113785791..113786752-chr5:114405185..114405973,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1026006	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11241313	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11241314	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11241315	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12186657	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12188014	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12188143	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12189322	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2974503	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2974511	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2974513	0.89[ASN][1000 genomes]
rs55638352	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55799813	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55898517	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55927006	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56250025	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62380016	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62380051	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62380053	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6859538	0.89[ASN][1000 genomes]
rs6881197	0.89[ASN][1000 genomes]
rs72811756	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706928	0.92[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	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1029048	chr5:114345201-114408136	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv519235	chr5:114404806-114407661	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114405400-114406600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr5:114405600-114407600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:114405600-114408200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr5:114405600-114408200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:114405800-114408000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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