Variant report

Variant	rs2417291
Chromosome Location	chr9:104467064-104467065
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	chr9:104463930..104467725-chr9:104467754..104469771,4	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10512283	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10512284	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10512286	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819954	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819955	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819956	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819958	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819959	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819961	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10819977	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989572	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989592	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989594	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989596	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989597	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989598	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10989605	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12338602	0.84[EUR][1000 genomes]
rs12708308	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1323427	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13289501	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1337684	0.84[EUR][1000 genomes]
rs1407873	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1407874	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17197124	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17199066	1.00[ASN][1000 genomes]
rs1853447	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2225879	0.84[EUR][1000 genomes]
rs34360878	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34888126	0.92[ASN][1000 genomes]
rs35227408	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35569161	0.92[ASN][1000 genomes]
rs4266702	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4442195	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4743484	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55749212	0.92[ASN][1000 genomes]
rs56052939	0.92[ASN][1000 genomes]
rs6479060	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745355	0.92[ASN][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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1046590	chr9:104450624-104848588	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104459000-104467200	Weak transcription	Liver	Liver
2	chr9:104465000-104467200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr9:104465800-104467200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr9:104466800-104467200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:104466800-104467200	Enhancers	Duodenum Mucosa	Duodenum
6	chr9:104466800-104467400	Enhancers	Fetal Lung	lung
7	chr9:104467000-104467200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:104467000-104467200	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr9:104467000-104467400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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