Variant report

Variant	rs10513232
Chromosome Location	chr3:143603535-143603536
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	chr3:143601941..143604638-chr3:143689903..143691740,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181744	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10513230	0.93[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513231	1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11920369	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1394403	0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1504605	0.85[JPT][hapmap];1.00[EUR][1000 genomes]
rs16854417	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854421	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854423	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854424	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854463	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854493	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16854525	0.89[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs16854588	0.89[ASN][1000 genomes]
rs16854594	0.95[ASN][1000 genomes]
rs16854639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17275413	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1823220	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2361199	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs3935024	0.95[ASN][1000 genomes]
rs4839613	1.00[JPT][hapmap]
rs4839614	0.89[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap]
rs4839659	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4839660	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4839661	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4839663	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs55734708	0.93[ASN][1000 genomes]
rs56954087	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57853180	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58917148	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59089060	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60230497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60765943	0.90[ASN][1000 genomes]
rs61195916	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61534234	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61574504	0.88[ASN][1000 genomes]
rs6440202	0.85[JPT][hapmap]
rs6765414	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6769847	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6792031	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6799226	0.82[JPT][hapmap];1.00[EUR][1000 genomes]
rs6804065	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs73010566	0.89[ASN][1000 genomes]
rs73871853	0.93[ASN][1000 genomes]
rs73871854	0.93[ASN][1000 genomes]
rs73871855	0.93[ASN][1000 genomes]
rs73871858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73871859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73871860	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73871861	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73871863	1.00[EUR][1000 genomes]
rs73871864	1.00[EUR][1000 genomes]
rs7651412	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7652644	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs924851	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs951594	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs951595	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9822158	0.89[CHB][hapmap];1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009935	chr3:143497700-143610852	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143602600-143607200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:143603400-143603600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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