Variant report

Variant	rs10114756
Chromosome Location	chr9:85010918-85010919
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:85009985..85011686-chr9:85015834..85018239,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10113923	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10123160	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10124221	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10125999	0.95[CEU][hapmap];0.86[CHB][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10512125	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11139564	0.90[ASN][1000 genomes]
rs11139566	0.93[EUR][1000 genomes]
rs11139569	0.82[JPT][hapmap]
rs11139570	0.96[EUR][1000 genomes]
rs12002791	0.86[EUR][1000 genomes]
rs12002792	0.83[EUR][1000 genomes]
rs12551735	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12684886	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13290374	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1411662	0.80[CEU][hapmap]
rs2378631	0.91[ASN][1000 genomes]
rs28520227	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2889949	0.95[CEU][hapmap];0.82[JPT][hapmap];0.96[EUR][1000 genomes]
rs34637520	0.96[EUR][1000 genomes]
rs35501117	0.92[EUR][1000 genomes]
rs3892417	0.90[CEU][hapmap];0.82[JPT][hapmap]
rs4465043	0.88[ASN][1000 genomes]
rs4877232	0.94[EUR][1000 genomes]
rs4877233	0.80[CEU][hapmap]
rs4877692	0.95[EUR][1000 genomes]
rs4877693	0.85[CEU][hapmap]
rs7018522	0.82[JPT][hapmap]
rs7048894	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7048952	0.89[ASN][1000 genomes]
rs7854052	0.95[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs7869176	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7874021	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7874946	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893507	chr9:84799537-85097651	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893508	chr9:84954592-85080395	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv893509	chr9:84954592-85097651	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893510	chr9:84954592-85117420	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85010600-85011000	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