Variant report

Variant	rs2721252
Chromosome Location	chr8:87156172-87156173
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:87153151..87158884-chr8:87159008..87162555,5	MCF-7	breast:
2	chr8:87154721..87156473-chr8:87354419..87356227,3	MCF-7	breast:
3	chr6:17392280..17394082-chr8:87153863..87156239,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254231	Chromatin interaction
ENSG00000123124	Chromatin interaction
ENSG00000112186	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10097379	0.85[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];0.88[TSI][hapmap]
rs10098631	0.82[JPT][hapmap]
rs10099368	0.82[JPT][hapmap]
rs10102252	0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs10103166	0.81[CHD][hapmap];0.86[JPT][hapmap]
rs10106391	0.82[JPT][hapmap]
rs10106497	0.86[JPT][hapmap]
rs10112076	0.82[JPT][hapmap]
rs10112474	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs10504819	0.81[JPT][hapmap]
rs11988449	0.81[JPT][hapmap]
rs12541053	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs12546618	0.86[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs13254996	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap]
rs13257877	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs13262822	0.84[CHD][hapmap];0.82[JPT][hapmap]
rs13265507	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs13267067	0.82[JPT][hapmap]
rs13272356	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs13280528	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs13281890	0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs13282492	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs1384878	0.81[JPT][hapmap]
rs1384879	0.81[JPT][hapmap]
rs16887456	0.82[JPT][hapmap]
rs2318396	0.82[JPT][hapmap]
rs2626325	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2626333	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2626335	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2626337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2626338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2626341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2626343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[ASN][1000 genomes]
rs2721248	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2721254	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2721255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2976187	0.82[CHD][hapmap];0.80[GIH][hapmap];0.82[JPT][hapmap];0.80[MEX][hapmap]
rs2976190	0.81[CHD][hapmap];0.80[GIH][hapmap];0.82[JPT][hapmap]
rs4076881	0.87[CHB][hapmap];0.82[CHD][hapmap];0.95[JPT][hapmap]
rs4311641	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs4443642	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs4571715	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs4960953	0.81[JPT][hapmap]
rs4960955	0.81[JPT][hapmap]
rs4960959	0.82[JPT][hapmap]
rs4961077	0.81[JPT][hapmap]
rs4961092	0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs6470428	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs6470714	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs6470733	0.86[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs6990782	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6993377	0.81[JPT][hapmap]
rs6996246	0.85[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs6999252	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7001674	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs7001699	0.90[JPT][hapmap]
rs7016268	0.86[JPT][hapmap]
rs7017607	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap]
rs7350116	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs7821560	0.86[JPT][hapmap]
rs7836003	0.80[JPT][hapmap]
rs7837251	0.82[JPT][hapmap]
rs9643132	0.81[JPT][hapmap]
rs9643143	0.86[JPT][hapmap]
rs975817	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][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	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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87155600-87156400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:87156000-87156400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:87156000-87156600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:87156000-87156600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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