Variant report

Variant	rs12156646
Chromosome Location	chr9:96682767-96682768
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	chr9:96676732..96679654-chr9:96681245..96683320,2	MCF-7	breast:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10821265	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821266	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821268	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821269	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821270	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10821271	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992983	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992985	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992986	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992987	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10992988	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10992989	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10992990	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10992991	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10992993	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12002825	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12156572	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12156575	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12156596	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12375881	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12377040	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12377238	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12683201	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12683978	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12684253	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12685500	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12685752	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16909596	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1890382	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1933676	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1933677	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2095776	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2153068	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2153069	0.88[ASN][1000 genomes]
rs55984014	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56023244	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56056624	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56149416	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56218521	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56310704	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56677923	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57777894	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58261080	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59292216	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59635608	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59731822	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59853604	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59879437	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60396345	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60508020	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60708208	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60812510	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60942558	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61433932	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66667702	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67006132	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67569294	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7023513	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7028921	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7038359	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7039765	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7042729	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73517149	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7858507	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7860425	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7861231	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7875295	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7875690	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893589	chr9:96624645-96884544	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1053137	chr9:96644876-96683214	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1046904	chr9:96647940-96689327	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1035418	chr9:96647940-96711409	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	esv1801607	chr9:96657324-96683214	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1042043	chr9:96657324-96689327	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96677000-96685200	Weak transcription	Spleen	Spleen
2	chr9:96680200-96687200	Weak transcription	Gastric	stomach
3	chr9:96681400-96690600	Weak transcription	Right Atrium	heart
4	chr9:96682200-96684000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr9:96682400-96683000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:96682400-96683000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr9:96682600-96684800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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