Variant report

Variant	rs932209
Chromosome Location	chr4:142588447-142588448
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	chr4:142586443..142587982-chr4:142588038..142590798,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1027280	0.87[EUR][1000 genomes]
rs1027281	0.86[EUR][1000 genomes]
rs1057972	0.85[EUR][1000 genomes]
rs12508335	0.89[EUR][1000 genomes]
rs12508866	1.00[JPT][hapmap]
rs12510030	0.88[EUR][1000 genomes]
rs13112582	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs13117878	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13122930	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs13123506	0.90[EUR][1000 genomes]
rs13126364	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13139573	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs1493022	0.86[EUR][1000 genomes]
rs1493025	0.85[EUR][1000 genomes]
rs1519551	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1602774	0.87[EUR][1000 genomes]
rs1602775	0.87[EUR][1000 genomes]
rs17007610	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs1873822	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs2030326	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2090664	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.91[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2139383	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs2291596	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs2322300	0.89[EUR][1000 genomes]
rs2322301	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs2322302	0.87[EUR][1000 genomes]
rs2857261	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs4104674	0.86[EUR][1000 genomes]
rs4245934	0.86[EUR][1000 genomes]
rs4530709	0.90[EUR][1000 genomes]
rs4597912	0.87[EUR][1000 genomes]
rs55849760	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6537060	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs6537061	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs6537062	0.82[EUR][1000 genomes]
rs6537063	0.87[EUR][1000 genomes]
rs6537064	0.87[EUR][1000 genomes]
rs6537070	0.86[EUR][1000 genomes]
rs6812078	0.86[EUR][1000 genomes]
rs6819823	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs6831361	0.87[EUR][1000 genomes]
rs6847434	0.90[EUR][1000 genomes]
rs6852617	0.87[EUR][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	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1030822	chr4:142487721-142706053	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1027004	chr4:142487721-143007320	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142575400-142589400	Weak transcription	Aorta	Aorta
2	chr4:142576400-142592600	Weak transcription	Psoas Muscle	Psoas
3	chr4:142576400-142598600	Weak transcription	Left Ventricle	heart
4	chr4:142579800-142589600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr4:142580600-142589400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:142581400-142589600	Weak transcription	A549	lung
7	chr4:142583400-142634600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:142586400-142589400	Weak transcription	Pancreas	Pancrea

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