Variant report

Variant	rs28701878
Chromosome Location	chr14:81587505-81587506
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	chr14:81586845..81589081-chr14:81590020..81592537,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10131452	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10131719	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10133928	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10142430	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10147462	0.87[ASN][1000 genomes]
rs12323385	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17111530	0.94[ASN][1000 genomes]
rs2273845	0.87[ASN][1000 genomes]
rs2284737	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2300537	0.85[ASN][1000 genomes]
rs28491084	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28507187	0.89[ASN][1000 genomes]
rs28640259	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28661095	0.89[ASN][1000 genomes]
rs28730923	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3783938	0.99[ASN][1000 genomes]
rs3783940	1.00[ASN][1000 genomes]
rs59500227	0.97[ASN][1000 genomes]
rs59645772	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6574628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150881	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627193	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627195	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627196	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627197	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72627198	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8020489	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[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	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81538200-81593000	Weak transcription	Psoas Muscle	Psoas
2	chr14:81572600-81591400	Weak transcription	Liver	Liver
3	chr14:81579800-81591800	Weak transcription	Thymus	Thymus
4	chr14:81579800-81591800	Weak transcription	Dnd41	blood
5	chr14:81581000-81593200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:81586400-81589800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:81586800-81592200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr14:81587000-81587600	Enhancers	Brain Substantia Nigra	brain
9	chr14:81587400-81587800	Enhancers	Primary B cells from cord blood	blood
10	chr14:81587400-81588800	Enhancers	Monocytes-CD14+_RO01746	blood

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