Variant report

Variant	rs10072292
Chromosome Location	chr5:57176069-57176070
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:57174384..57178460-chr5:57754428..57757205,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145632	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1347071	1.00[YRI][hapmap]
rs1821210	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1861059	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2408854	1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2568537	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4235475	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4235476	0.87[EUR][1000 genomes]
rs4285175	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4317282	1.00[AFR][1000 genomes]
rs4380607	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4403130	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4421067	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4458541	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4513644	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4699913	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4700231	1.00[AFR][1000 genomes]
rs4700233	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62362089	0.82[AFR][1000 genomes]
rs6450442	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6450444	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6896848	1.00[AFR][1000 genomes]
rs702699	0.84[AFR][1000 genomes]
rs702701	1.00[AFR][1000 genomes]
rs7701200	0.83[EUR][1000 genomes]
rs854024	1.00[AFR][1000 genomes]
rs854028	1.00[AFR][1000 genomes]
rs854031	1.00[AFR][1000 genomes]
rs854033	1.00[AFR][1000 genomes]
rs854035	1.00[AFR][1000 genomes]
rs854036	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs854045	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs854046	1.00[AFR][1000 genomes]
rs854048	1.00[AFR][1000 genomes]
rs854049	1.00[AFR][1000 genomes]
rs854050	1.00[AFR][1000 genomes]
rs854053	1.00[AFR][1000 genomes]
rs868049	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs897264	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57175000-57185200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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