Variant report

Variant	rs3891859
Chromosome Location	chr5:96691804-96691805
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10044182	0.93[CEU][hapmap]
rs1018058	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10476561	0.84[EUR][1000 genomes]
rs10515256	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs11743991	0.81[EUR][1000 genomes]
rs11746308	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13171520	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs1423501	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs1423502	0.93[CEU][hapmap]
rs1423503	0.89[CEU][hapmap]
rs1423504	0.89[CEU][hapmap]
rs1528593	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1528598	0.87[EUR][1000 genomes]
rs1528599	0.87[EUR][1000 genomes]
rs1581662	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17630601	0.96[CEU][hapmap];0.83[EUR][1000 genomes]
rs17630655	0.84[EUR][1000 genomes]
rs1845649	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1845652	0.92[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.94[YRI][hapmap];0.85[EUR][1000 genomes]
rs1862593	0.84[EUR][1000 genomes]
rs1874292	0.81[EUR][1000 genomes]
rs2081143	0.87[EUR][1000 genomes]
rs2088150	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2222767	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2463784	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2548419	0.87[EUR][1000 genomes]
rs2548426	0.88[EUR][1000 genomes]
rs2548427	0.88[EUR][1000 genomes]
rs2643487	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643490	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643491	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643492	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643493	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643494	0.88[EUR][1000 genomes]
rs2643495	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643497	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643498	0.80[EUR][1000 genomes]
rs2643500	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2643531	0.88[EUR][1000 genomes]
rs2643532	0.88[EUR][1000 genomes]
rs2643567	0.88[EUR][1000 genomes]
rs2697569	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697570	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697575	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697576	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697577	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697578	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697579	0.83[EUR][1000 genomes]
rs2697580	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697581	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697582	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2697599	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697600	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697601	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697602	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697603	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697604	0.80[EUR][1000 genomes]
rs2697605	0.80[EUR][1000 genomes]
rs2697606	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697610	0.83[EUR][1000 genomes]
rs2697611	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2697644	0.88[EUR][1000 genomes]
rs291806	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs291807	0.81[ASN][1000 genomes]
rs291808	0.81[ASN][1000 genomes]
rs291811	0.81[ASN][1000 genomes]
rs291812	0.81[ASN][1000 genomes]
rs3108531	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3108532	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34089335	0.84[EUR][1000 genomes]
rs34985391	0.81[ASN][1000 genomes]
rs35498938	0.83[EUR][1000 genomes]
rs36154380	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4242236	0.83[CEU][hapmap]
rs4869154	0.84[EUR][1000 genomes]
rs4869155	0.84[EUR][1000 genomes]
rs4869324	0.92[CEU][hapmap]
rs4869345	0.84[ASN][1000 genomes]
rs56267018	0.81[EUR][1000 genomes]
rs6861811	0.93[CEU][hapmap]
rs6891107	0.84[AMR][1000 genomes]
rs6895915	0.84[AMR][1000 genomes]
rs721801	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72777631	0.82[EUR][1000 genomes]
rs72777640	0.83[EUR][1000 genomes]
rs72777653	0.84[EUR][1000 genomes]
rs7729001	0.84[EUR][1000 genomes]
rs9314195	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1019790	chr5:96471680-96980633	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv537812	chr5:96471680-96980633	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv534326	chr5:96531217-97283481	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv882394	chr5:96538585-97108559	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1032548	chr5:96565121-97046804	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv537813	chr5:96565121-97046804	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv830415	chr5:96597763-96764157	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv598964	chr5:96612401-96705762	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1025654	chr5:96613448-96817528	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96691200-96692200	Flanking Active TSS	GM12878-XiMat	blood

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