Variant report

Variant	rs451121
Chromosome Location	chr21:17374964-17374965
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	chr21:17374756..17375589-chr21:17702524..17703193,2	MCF-7	breast:
2	chr21:17374904..17375409-chr21:17702413..17703119,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000215386	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11088561	0.84[ASN][1000 genomes]
rs12482831	0.81[ASN][1000 genomes]
rs12483563	0.83[ASN][1000 genomes]
rs12483594	0.83[ASN][1000 genomes]
rs12483611	0.83[ASN][1000 genomes]
rs1740137	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1893382	0.83[ASN][1000 genomes]
rs1893383	0.83[ASN][1000 genomes]
rs2205453	0.91[ASN][1000 genomes]
rs2404032	0.91[ASN][1000 genomes]
rs2823533	0.89[ASN][1000 genomes]
rs2823534	0.91[ASN][1000 genomes]
rs2823535	0.91[ASN][1000 genomes]
rs2823536	0.91[ASN][1000 genomes]
rs2823537	0.91[ASN][1000 genomes]
rs2823538	0.91[ASN][1000 genomes]
rs2823539	0.91[ASN][1000 genomes]
rs2823540	0.91[ASN][1000 genomes]
rs2823542	0.91[ASN][1000 genomes]
rs2823543	0.91[ASN][1000 genomes]
rs2823545	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2823546	0.80[ASN][1000 genomes]
rs2823549	0.83[ASN][1000 genomes]
rs2823550	0.83[ASN][1000 genomes]
rs2896726	0.91[ASN][1000 genomes]
rs366613	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs368760	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs375736	0.84[ASN][1000 genomes]
rs387709	0.84[ASN][1000 genomes]
rs388509	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs390503	0.91[ASN][1000 genomes]
rs399959	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs400590	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs405703	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs407058	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs412399	0.89[ASN][1000 genomes]
rs417411	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs419827	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs419867	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs420519	0.91[ASN][1000 genomes]
rs420571	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs420806	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs422504	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs433721	0.97[ASN][1000 genomes]
rs435166	0.91[ASN][1000 genomes]
rs444574	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs447456	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs447842	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs453844	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs457319	0.83[ASN][1000 genomes]
rs459355	0.83[ASN][1000 genomes]
rs56110468	0.83[ASN][1000 genomes]
rs6517682	0.83[ASN][1000 genomes]
rs7277086	0.82[ASN][1000 genomes]
rs7279935	0.88[ASN][1000 genomes]
rs9979920	0.81[ASN][1000 genomes]

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	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 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	chr21:17369000-17376000	Weak transcription	Osteobl	bone
2	chr21:17370800-17376000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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