Variant report

Variant	rs74086993
Chromosome Location	chr1:71351303-71351304
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	chr1:71350292..71353402-chr1:71355074..71357779,3	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10889891	0.84[ASN][1000 genomes]
rs11209705	0.86[ASN][1000 genomes]
rs11803673	0.84[ASN][1000 genomes]
rs11810467	0.86[ASN][1000 genomes]
rs12026099	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12026456	0.86[ASN][1000 genomes]
rs12034333	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12040186	0.86[ASN][1000 genomes]
rs12049445	0.86[ASN][1000 genomes]
rs17131473	0.91[ASN][1000 genomes]
rs17131476	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131485	0.94[ASN][1000 genomes]
rs17131487	0.93[AFR][1000 genomes]
rs2068652	0.94[ASN][1000 genomes]
rs34087524	0.88[ASN][1000 genomes]
rs34745168	0.88[ASN][1000 genomes]
rs34999609	0.90[AFR][1000 genomes]
rs35368675	0.90[AFR][1000 genomes]
rs35615554	0.88[ASN][1000 genomes]
rs35799180	0.90[AFR][1000 genomes]
rs36021131	0.94[ASN][1000 genomes]
rs55884889	0.95[ASN][1000 genomes]
rs58659672	0.93[AFR][1000 genomes]
rs6661453	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6684573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74086786	0.85[ASN][1000 genomes]
rs74086973	0.89[ASN][1000 genomes]
rs74086974	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74086976	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74086980	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74086985	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74089104	0.93[AFR][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	esv1845198	chr1:71274759-71514969	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv830148	chr1:71310366-71483932	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71346000-71357000	Weak transcription	Adipose Nuclei	Adipose
2	chr1:71348200-71354400	Weak transcription	Aorta	Aorta
3	chr1:71350400-71352200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links