Variant report

Variant	rs1026096
Chromosome Location	chr12:63401362-63401363
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:63394199..63396299-chr12:63400544..63402068,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257779	Chromatin interaction

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

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

rs_ID	r²[population]
rs10506470	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249935	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12813083	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12821413	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12821849	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12829134	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098568	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17098575	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17098581	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17098689	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098761	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098763	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098774	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098779	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098789	1.00[ASN][1000 genomes]
rs17098794	1.00[ASN][1000 genomes]
rs1731661	1.00[ASN][1000 genomes]
rs17739095	1.00[ASN][1000 genomes]
rs2464118	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2840070	1.00[ASN][1000 genomes]
rs2884542	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34203667	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35910451	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67784802	1.00[ASN][1000 genomes]
rs67994077	1.00[ASN][1000 genomes]
rs699591	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs699593	1.00[ASN][1000 genomes]
rs699615	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699618	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs71450600	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71465172	1.00[ASN][1000 genomes]
rs71465180	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71465181	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs771974	1.00[CEU][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs771976	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs772538	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs772541	1.00[ASN][1000 genomes]
rs9971730	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	esv3415227	chr12:63228121-63591615	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1046836	chr12:63392391-64377169	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 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	chr12:63400800-63401600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr12:63401200-63401600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links