Variant report

Variant	rs296674
Chromosome Location	chr9:93715476-93715477
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:93681274..93683060-chr9:93714729..93717613,2	MCF-7	breast:
2	chr9:93714100..93716196-chr9:94186496..94188571,2	MCF-7	breast:
3	chr9:93677133..93677996-chr9:93715404..93716043,2	MCF-7	breast:
4	chr9:93677729..93678282-chr9:93715398..93716120,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000233081	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1041381	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1330682	1.00[CEU][hapmap]
rs158683	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1675292	0.91[EUR][1000 genomes]
rs1675293	0.91[EUR][1000 genomes]
rs1675294	1.00[CEU][hapmap]
rs1675295	0.91[EUR][1000 genomes]
rs1675296	0.91[EUR][1000 genomes]
rs1675297	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1675298	0.91[EUR][1000 genomes]
rs1675302	0.91[EUR][1000 genomes]
rs1675303	0.91[EUR][1000 genomes]
rs1675305	0.91[EUR][1000 genomes]
rs1675306	0.91[EUR][1000 genomes]
rs1675307	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs169743	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1755982	0.91[EUR][1000 genomes]
rs1755983	0.91[EUR][1000 genomes]
rs184114	0.91[EUR][1000 genomes]
rs190029	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2774255	0.91[EUR][1000 genomes]
rs291746	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs291747	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs291749	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs291752	0.91[EUR][1000 genomes]
rs291754	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs291755	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs291757	0.91[EUR][1000 genomes]
rs291758	0.83[EUR][1000 genomes]
rs291759	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs291761	0.91[EUR][1000 genomes]
rs291763	0.91[EUR][1000 genomes]
rs296653	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs296654	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs296656	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs296658	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs296659	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs296660	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs296662	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs296670	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs296675	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs296678	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs296685	1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs296687	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs296689	1.00[EUR][1000 genomes]
rs296692	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs296694	0.90[EUR][1000 genomes]
rs296697	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs296704	1.00[EUR][1000 genomes]
rs296705	1.00[EUR][1000 genomes]
rs296707	0.91[EUR][1000 genomes]
rs296712	0.91[EUR][1000 genomes]
rs296720	0.91[EUR][1000 genomes]
rs296723	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs296727	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs296729	0.81[EUR][1000 genomes]
rs364622	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs376648	1.00[EUR][1000 genomes]
rs390574	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs426365	1.00[EUR][1000 genomes];0.83[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	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93712800-93717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:93713400-93720400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:93715200-93715800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr9:93715200-93716000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:93715200-93716200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr9:93715400-93716200	Enhancers	HUES48 Cell Line	embryonic stem cell

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