Variant report

Variant	rs6731454
Chromosome Location	chr2:212443436-212443437
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	chr2:212443336..212445425-chr2:212453184..212455748,2	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1009142	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10210942	0.84[ASN][1000 genomes]
rs10804199	0.86[ASN][1000 genomes]
rs10932386	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11679779	0.96[ASN][1000 genomes]
rs11679860	0.96[ASN][1000 genomes]
rs11687988	0.96[ASN][1000 genomes]
rs11691078	0.94[ASN][1000 genomes]
rs11695852	0.92[ASN][1000 genomes]
rs12465773	0.86[ASN][1000 genomes]
rs12614500	0.88[ASN][1000 genomes]
rs12619171	0.90[ASN][1000 genomes]
rs12694243	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12694245	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13007756	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1818751	0.90[ASN][1000 genomes]
rs1829610	0.86[ASN][1000 genomes]
rs1829611	0.84[ASN][1000 genomes]
rs1965462	0.83[ASN][1000 genomes]
rs1972143	0.84[ASN][1000 genomes]
rs1976834	0.94[ASN][1000 genomes]
rs2371303	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2371304	0.96[ASN][1000 genomes]
rs2371305	0.94[ASN][1000 genomes]
rs2888004	0.87[ASN][1000 genomes]
rs4488593	0.96[ASN][1000 genomes]
rs4599046	0.96[ASN][1000 genomes]
rs4640322	0.90[ASN][1000 genomes]
rs4672619	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4673623	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4673624	0.88[ASN][1000 genomes]
rs6721804	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6746549	0.80[EUR][1000 genomes]
rs7561282	0.90[ASN][1000 genomes]
rs7572669	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7595207	0.90[ASN][1000 genomes]
rs7595223	0.90[ASN][1000 genomes]
rs7602757	0.85[EUR][1000 genomes]
rs7602850	0.80[EUR][1000 genomes]
rs9288434	0.84[ASN][1000 genomes]
rs9288435	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000722	chr2:212272622-212465143	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv460069	chr2:212415948-212471642	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv584320	chr2:212415948-212471642	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212419400-212451800	Weak transcription	Aorta	Aorta
2	chr2:212435400-212450000	Weak transcription	Fetal Heart	heart
3	chr2:212443200-212444400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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