Variant report

Variant	rs7005074
Chromosome Location	chr8:87163035-87163036
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:87159732..87163307-chr8:87354043..87356209,3	MCF-7	breast:
2	chr8:87161416..87164827-chr8:87354459..87357124,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000123124	Chromatin interaction
ENSG00000254231	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10504820	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs10504821	0.95[CEU][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10808536	0.90[EUR][1000 genomes]
rs10808539	0.87[CEU][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes]
rs10956194	0.94[JPT][hapmap]
rs11784259	0.90[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap]
rs12550469	0.88[JPT][hapmap]
rs12550770	0.81[JPT][hapmap]
rs12677686	0.88[JPT][hapmap]
rs13263240	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1483779	0.94[JPT][hapmap]
rs17605526	0.94[JPT][hapmap]
rs1872136	0.94[JPT][hapmap]
rs2128930	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2466326	0.94[JPT][hapmap]
rs2626324	0.94[JPT][hapmap]
rs2626326	0.94[JPT][hapmap]
rs2626327	0.94[JPT][hapmap]
rs2626328	0.94[JPT][hapmap]
rs2626329	0.94[JPT][hapmap]
rs2626331	0.94[JPT][hapmap]
rs2626332	0.94[JPT][hapmap]
rs2626339	0.93[JPT][hapmap]
rs2626340	0.94[JPT][hapmap]
rs2626342	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2626344	0.84[ASN][1000 genomes]
rs2626345	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2721244	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2721246	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2721247	0.84[ASN][1000 genomes]
rs2721249	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2721250	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2721251	0.94[JPT][hapmap]
rs2721253	0.94[JPT][hapmap]
rs2721256	0.94[JPT][hapmap]
rs2721257	0.94[JPT][hapmap]
rs2721260	0.94[JPT][hapmap]
rs4333573	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4442123	0.84[ASN][1000 genomes]
rs4584126	0.91[CEU][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4599790	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4961081	0.81[JPT][hapmap]
rs6469859	0.88[JPT][hapmap]
rs6981984	0.88[JPT][hapmap]
rs6983781	0.91[CEU][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6992915	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs6994457	0.88[JPT][hapmap]
rs7011724	0.84[ASN][1000 genomes]
rs7820770	0.87[CEU][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7845147	0.88[JPT][hapmap]
rs953147	0.94[JPT][hapmap]
rs953148	0.94[JPT][hapmap]
rs9693993	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9694211	0.92[EUR][1000 genomes]
rs975818	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428204	chr8:86405478-87312208	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv529563	chr8:86467090-87381984	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv932023	chr8:86845979-87490694	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv891147	chr8:86886950-87333968	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv891149	chr8:87023306-87167184	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1034855	chr8:87040075-87168730	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	esv2761443	chr8:87109368-87170814	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1020115	chr8:87111707-87167790	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1026646	chr8:87111707-87177368	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv611674	chr8:87156172-87315920	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1027648	chr8:87161437-87319476	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv429926	chr8:87161695-87429872	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87162400-87163200	Enhancers	Gastric	stomach
2	chr8:87162800-87163200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:87162800-87165600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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