Variant report

Variant	rs9495502
Chromosome Location	chr6:139818658-139818659
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:139808542..139810707-chr6:139817260..139819598,2	MCF-7	breast:
2	chr6:139817301..139819044-chr6:139820730..139822475,2	K562	blood:
3	chr6:139818335..139820226-chr6:139826249..139828991,2	K562	blood:
4	chr6:139732315..139735138-chr6:139816703..139819497,2	K562	blood:
5	chr6:139692857..139697626-chr6:139818294..139823547,7	K562	blood:
6	chr6:139818335..139820226-chr6:139825228..139828991,3	K562	blood:

Variant related genes	Relation type
ENSG00000164442	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10872516	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11155070	0.81[AMR][1000 genomes]
rs1468708	0.84[JPT][hapmap];0.81[AMR][1000 genomes]
rs1468709	0.84[JPT][hapmap];0.82[YRI][hapmap];0.83[AMR][1000 genomes]
rs2908512	0.94[ASN][1000 genomes]
rs2908513	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2908517	0.88[ASN][1000 genomes]
rs3010285	0.85[ASN][1000 genomes]
rs3010286	0.84[JPT][hapmap];0.81[YRI][hapmap]
rs4896461	0.81[AMR][1000 genomes]
rs4896463	0.84[JPT][hapmap];0.83[AMR][1000 genomes]
rs4896464	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs618652	0.80[ASN][1000 genomes]
rs6570344	0.81[AMR][1000 genomes]
rs6916887	0.81[AMR][1000 genomes]
rs6923416	0.84[JPT][hapmap];0.81[AMR][1000 genomes]
rs6926031	0.81[AMR][1000 genomes]
rs71543295	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7770257	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376420	0.84[JPT][hapmap];0.82[AMR][1000 genomes]
rs9376421	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9376422	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9376423	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9389689	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9399282	0.84[JPT][hapmap];0.81[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9403080	0.84[JPT][hapmap];0.82[YRI][hapmap];0.83[AMR][1000 genomes]
rs9403081	0.88[EUR][1000 genomes]
rs9403082	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403083	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403084	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1026819	chr6:139813809-139834012	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139815800-139822800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:139817600-139820200	Enhancers	Pancreas	Pancrea
3	chr6:139818000-139819000	Flanking Active TSS	K562	blood
4	chr6:139818200-139820000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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