Variant report

Variant	rs487219
Chromosome Location	chr10:27554345-27554346
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:27531009..27532582-chr10:27554298..27557001,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000262412	Chromatin interaction
ENSG00000107897	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10764674	1.00[AMR][1000 genomes]
rs10829210	1.00[AMR][1000 genomes]
rs11015569	1.00[AMR][1000 genomes]
rs1148168	1.00[AMR][1000 genomes]
rs1148170	1.00[AMR][1000 genomes]
rs1630674	1.00[AMR][1000 genomes]
rs1753410	1.00[AMR][1000 genomes]
rs1755400	1.00[AMR][1000 genomes]
rs1755402	1.00[AMR][1000 genomes]
rs1775355	1.00[AMR][1000 genomes]
rs1887824	1.00[AMR][1000 genomes]
rs2479910	1.00[AMR][1000 genomes]
rs2479913	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2479916	1.00[AMR][1000 genomes]
rs2480716	1.00[AMR][1000 genomes]
rs2480717	1.00[AMR][1000 genomes]
rs2489371	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3118890	1.00[AMR][1000 genomes]
rs4747591	1.00[AMR][1000 genomes]
rs493598	1.00[AMR][1000 genomes]
rs525441	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs530567	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56030738	1.00[AMR][1000 genomes]
rs605028	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs605354	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs607717	1.00[AMR][1000 genomes]
rs60918938	1.00[AMR][1000 genomes]
rs620401	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs641128	1.00[AMR][1000 genomes]
rs646612	1.00[AMR][1000 genomes]
rs658082	1.00[AMR][1000 genomes]
rs695044	1.00[AMR][1000 genomes]
rs7082922	1.00[AMR][1000 genomes]
rs7095372	1.00[AMR][1000 genomes]
rs788200	1.00[AMR][1000 genomes]
rs788206	1.00[AMR][1000 genomes]
rs788213	1.00[AMR][1000 genomes]
rs788217	1.00[AMR][1000 genomes]
rs788224	1.00[AMR][1000 genomes]
rs788225	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs788231	1.00[AMR][1000 genomes]
rs788233	1.00[AMR][1000 genomes]
rs788236	1.00[AMR][1000 genomes]
rs788238	1.00[AMR][1000 genomes]
rs796842	1.00[AMR][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	esv2422253	chr10:27431366-27575370	Strong transcription Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3337781	chr10:27472216-27666703	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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