Variant report

Variant	rs383126
Chromosome Location	chr9:107976959-107976960
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	chr9:107976686..107978196-chr9:108005195..108008055,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000070214	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10120310	1.00[ASN][1000 genomes]
rs10820792	0.90[CHB][hapmap]
rs10820795	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs10991598	0.90[CHB][hapmap]
rs10991600	0.89[CHB][hapmap]
rs10991601	0.90[CHB][hapmap]
rs10991611	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs10991612	0.90[CHB][hapmap]
rs10991617	0.90[CHB][hapmap]
rs10991618	0.90[CHB][hapmap]
rs12335779	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs12343137	1.00[ASN][1000 genomes]
rs12347364	0.90[CHB][hapmap]
rs12348136	0.90[CHB][hapmap]
rs170582	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs179177	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs182756	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs193007	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs193008	0.81[CHB][hapmap]
rs193009	0.90[CHB][hapmap]
rs2004725	0.90[CHB][hapmap]
rs2100044	0.90[CHB][hapmap]
rs227887	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs227888	0.90[CHB][hapmap]
rs2900397	0.90[CHB][hapmap]
rs327947	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327948	0.90[CHB][hapmap]
rs327950	0.90[CHB][hapmap]
rs327955	0.90[CHB][hapmap]
rs327956	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs327958	0.90[CHB][hapmap]
rs327959	0.90[CHB][hapmap]
rs327960	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327967	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327976	0.90[CHB][hapmap]
rs327982	0.90[CHB][hapmap]
rs327983	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327984	0.90[CHB][hapmap]
rs327985	0.88[CHB][hapmap]
rs327987	0.90[CHB][hapmap]
rs327990	0.90[CHB][hapmap]
rs327991	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327992	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs327993	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327995	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327997	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs327999	0.90[CHB][hapmap]
rs328006	0.90[CHB][hapmap]
rs328007	0.90[CHB][hapmap]
rs328008	0.90[CHB][hapmap]
rs328010	0.90[CHB][hapmap]
rs328012	0.90[CHB][hapmap];0.85[CHD][hapmap]
rs328013	0.90[CHB][hapmap];0.95[CHD][hapmap]
rs328014	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs328015	0.90[CHB][hapmap]
rs328018	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs328019	0.90[CHB][hapmap]
rs328022	0.90[CHB][hapmap]
rs364564	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs365629	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs366018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs372554	1.00[ASN][1000 genomes]
rs372747	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs375034	0.90[CHB][hapmap]
rs375371	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs376926	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs378467	0.90[CHB][hapmap]
rs378716	1.00[ASN][1000 genomes]
rs380104	0.90[CHB][hapmap]
rs383272	0.90[CHB][hapmap]
rs384924	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs384947	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs386565	0.90[CHB][hapmap]
rs390235	1.00[ASN][1000 genomes]
rs399707	1.00[ASN][1000 genomes]
rs401899	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs405704	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs409595	1.00[ASN][1000 genomes]
rs413598	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs416573	1.00[ASN][1000 genomes]
rs416641	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs420672	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs420717	0.90[CHB][hapmap]
rs421342	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs421495	1.00[ASN][1000 genomes]
rs422084	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs423477	1.00[ASN][1000 genomes]
rs424495	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs427497	0.98[ASN][1000 genomes]
rs435267	0.98[ASN][1000 genomes]
rs440290	0.90[CHB][hapmap];0.91[CHD][hapmap]
rs442605	0.90[CHB][hapmap]
rs443094	0.90[CHB][hapmap]
rs453041	0.98[ASN][1000 genomes]
rs453378	1.00[ASN][1000 genomes]
rs6479305	0.90[CHB][hapmap]
rs7020982	0.81[CHB][hapmap];0.91[CHD][hapmap]
rs7021008	0.89[CHB][hapmap]
rs7039398	0.90[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046935	chr9:107414720-108028061	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1045108	chr9:107509553-108188550	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv893684	chr9:107893629-108001107	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv831678	chr9:107923522-108112813	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893685	chr9:107940737-108083485	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1043466	chr9:107950174-108001988	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv893686	chr9:107968330-108083485	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv893687	chr9:107973277-108083485	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv893688	chr9:107974761-108083485	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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