Variant report

Variant	rs4930360
Chromosome Location	chr11:66143247-66143248
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	chr11:66138896..66140491-chr11:66142378..66144405,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-867G23.8.1-6	chr11:66143019-66143451	expReg_chr11_6455_+

Variant related genes	Relation type
ENSG00000174669	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1039594	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1047029	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10750784	0.86[EUR][1000 genomes]
rs10791869	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10791872	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10791874	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10791876	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10896111	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10896112	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10896115	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10896116	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11227465	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11601396	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12416747	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12576293	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12576299	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12577196	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12785321	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12785651	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12786563	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12794121	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1546358	0.85[EUR][1000 genomes]
rs1785633	0.81[EUR][1000 genomes]
rs1892940	0.86[EUR][1000 genomes]
rs2279861	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2279862	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2282530	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3016767	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3177514	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34043951	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4244813	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4930177	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4930178	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4930179	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4930181	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4930362	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4930363	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4930366	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4930368	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55998145	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56123976	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56321771	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891449	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6591213	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6591215	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6591217	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs66810040	0.85[ASN][1000 genomes]
rs67780191	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7104253	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7104570	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7105015	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7105401	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7107191	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7110944	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7117630	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7126018	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73489638	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7938676	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7939111	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7940980	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs905770	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs947978	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	esv3407551	chr11:65794503-66158322	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	esv3392427	chr11:65981489-66273695	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
4	nsv897771	chr11:66011280-66362997	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	124 gene(s)	inside rSNPs	diseases
5	nsv897772	chr11:66018155-66254085	Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
6	nsv897780	chr11:66083129-66362997	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
7	nsv832193	chr11:66120339-66278805	Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4930360	RIN1	cis	Whole Blood	GTEx

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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