Variant report

Variant	rs7153182
Chromosome Location	chr14:38455293-38455294
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:38454795..38455310-chr14:38485447..38485994,2	MCF-7	breast:
2	chr14:38454830..38455672-chr14:38619407..38619954,2	MCF-7	breast:
3	chr14:38454845..38455414-chr14:38666225..38667085,2	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10134624	1.00[CEU][hapmap];0.88[GIH][hapmap];0.95[TSI][hapmap];0.96[EUR][1000 genomes]
rs10140719	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10145136	1.00[CEU][hapmap];0.88[GIH][hapmap];0.93[TSI][hapmap]
rs10145337	0.90[EUR][1000 genomes]
rs10146385	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs10483495	0.89[CEU][hapmap]
rs10872905	1.00[CEU][hapmap];0.80[AMR][1000 genomes]
rs1113092	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11156973	1.00[CEU][hapmap]
rs11156974	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11621735	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs11622986	0.96[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1170022	1.00[CEU][hapmap];0.80[TSI][hapmap]
rs1170023	0.92[CEU][hapmap]
rs1170024	0.93[EUR][1000 genomes]
rs1170025	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1170028	1.00[CEU][hapmap];0.88[TSI][hapmap];0.93[EUR][1000 genomes]
rs1170029	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1170030	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs1170031	0.89[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.83[MEX][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11851837	0.96[CEU][hapmap];0.81[CHB][hapmap]
rs12432452	1.00[CEU][hapmap]
rs12435640	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs12590816	0.96[CEU][hapmap]
rs12882516	1.00[CEU][hapmap]
rs17107343	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17179919	0.96[CEU][hapmap];0.82[CHB][hapmap];0.83[MEX][hapmap];0.82[EUR][1000 genomes]
rs17554993	1.00[CEU][hapmap];0.83[TSI][hapmap];0.90[EUR][1000 genomes]
rs1952787	0.96[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs1952788	0.96[CEU][hapmap]
rs1952790	0.82[CEU][hapmap]
rs1958692	0.82[CEU][hapmap]
rs1958693	1.00[CEU][hapmap]
rs1958694	1.00[CEU][hapmap]
rs1959676	1.00[CEU][hapmap]
rs2150322	0.96[CEU][hapmap];0.86[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.92[MEX][hapmap];0.86[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2183531	0.96[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.92[MEX][hapmap];0.86[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3809444	0.96[CEU][hapmap]
rs4143919	1.00[CEU][hapmap]
rs4322573	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.82[TSI][hapmap]
rs4597229	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs4898763	0.80[AMR][1000 genomes]
rs4898785	0.93[CEU][hapmap]
rs4901412	1.00[CEU][hapmap];0.80[AMR][1000 genomes]
rs4901421	0.96[CEU][hapmap]
rs4901422	0.96[CEU][hapmap]
rs4901423	0.96[CEU][hapmap]
rs6571829	0.96[CEU][hapmap]
rs6571830	0.96[CEU][hapmap]
rs71407747	0.81[EUR][1000 genomes]
rs7148370	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7155891	0.96[CEU][hapmap]
rs7158383	0.96[EUR][1000 genomes]
rs8005651	1.00[CEU][hapmap]
rs8005895	0.96[CEU][hapmap]
rs8013747	0.96[CEU][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs8014454	0.82[ASN][1000 genomes]
rs8014896	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8015738	1.00[CEU][hapmap];0.88[GIH][hapmap];0.95[TSI][hapmap]
rs8020796	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9322983	1.00[CEU][hapmap];0.83[TSI][hapmap]
rs954881	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9788473	0.96[CEU][hapmap]
rs9788476	0.96[CEU][hapmap]

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	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	nsv564387	chr14:38357864-38563111	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv901651	chr14:38419360-38556242	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr14:38455200-38455600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:38455200-38455600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:38455200-38455600	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr14:38455200-38455600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr14:38455200-38455600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr14:38455200-38455800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:38455200-38455800	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr14:38455200-38455800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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