Variant report

Variant	rs7010709
Chromosome Location	chr8:10701959-10701960
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:10696105..10699610-chr8:10701195..10704333,4	K562	blood:
2	chr8:10700359..10702352-chr8:10709225..10710771,2	K562	blood:
3	chr8:10695083..10698096-chr8:10698399..10704123,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253695	Chromatin interaction
ENSG00000254093	Chromatin interaction
ENSG00000258724	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10046628	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs10088888	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10089153	0.93[CHB][hapmap];0.84[CHD][hapmap]
rs10091386	0.87[CHB][hapmap]
rs10091961	0.86[EUR][1000 genomes]
rs10093774	0.87[CHB][hapmap];0.93[CHD][hapmap];0.80[ASN][1000 genomes]
rs10094907	1.00[YRI][hapmap]
rs10099021	1.00[YRI][hapmap]
rs10099137	0.86[YRI][hapmap]
rs10099928	1.00[YRI][hapmap]
rs10109034	1.00[YRI][hapmap]
rs10109416	0.87[CHB][hapmap]
rs10109550	1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.92[ASN][1000 genomes]
rs11250082	0.81[ASW][hapmap];1.00[CEU][hapmap];0.96[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11250083	0.87[CHB][hapmap];0.96[CHD][hapmap]
rs11776767	0.82[CHB][hapmap]
rs11986013	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11986015	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11990167	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12550169	1.00[YRI][hapmap]
rs1469556	0.87[CHB][hapmap];0.80[ASN][1000 genomes]
rs1469557	0.93[ASW][hapmap];1.00[CEU][hapmap];0.86[CHD][hapmap];0.96[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1544980	0.88[CEU][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1544981	0.85[ASW][hapmap];0.92[JPT][hapmap];0.82[MKK][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs1549794	0.93[YRI][hapmap]
rs1991650	0.87[CHB][hapmap];0.96[CHD][hapmap]
rs1991651	0.87[CHB][hapmap];0.93[CHD][hapmap]
rs2005311	0.84[CEU][hapmap]
rs2052963	0.85[ASW][hapmap];1.00[YRI][hapmap]
rs2271356	1.00[YRI][hapmap]
rs2271357	0.81[CHB][hapmap];0.86[CHD][hapmap]
rs2278335	0.87[CHB][hapmap];0.89[CHD][hapmap]
rs2292370	0.82[CHB][hapmap];0.89[CHD][hapmap]
rs2409650	0.80[CHB][hapmap]
rs2409651	1.00[YRI][hapmap]
rs28710808	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3808603	0.87[CHB][hapmap];0.93[CHD][hapmap]
rs3808605	0.95[ASN][1000 genomes]
rs4841452	0.85[CHB][hapmap]
rs60011038	0.83[ASN][1000 genomes]
rs6601524	0.85[ASW][hapmap];1.00[YRI][hapmap]
rs6601534	0.82[CHB][hapmap];0.86[CHD][hapmap]
rs6601536	0.87[CHB][hapmap];0.86[CHD][hapmap]
rs6982048	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6985218	1.00[YRI][hapmap]
rs6985890	0.92[ASN][1000 genomes]
rs6989846	1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[YRI][hapmap];0.92[ASN][1000 genomes]
rs6990055	0.82[CHB][hapmap]
rs6990589	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6991499	0.82[CHB][hapmap];0.86[CHD][hapmap]
rs6991526	0.82[CHB][hapmap]
rs6992366	0.81[CHB][hapmap];0.89[CHD][hapmap]
rs7000939	0.82[CHB][hapmap];0.86[CHD][hapmap]
rs7004998	0.82[CHB][hapmap];0.86[CHD][hapmap]
rs7005531	0.93[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs7010680	0.81[ASN][1000 genomes]
rs7013032	0.93[CHB][hapmap]
rs714371	0.93[YRI][hapmap]
rs7818181	0.87[CHB][hapmap];0.86[CHD][hapmap]
rs7823521	0.91[YRI][hapmap]
rs7824384	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.90[ASN][1000 genomes]
rs7826458	0.86[YRI][hapmap]
rs7829089	0.82[CHB][hapmap]
rs7830431	0.87[CHB][hapmap]
rs7833128	0.81[CHB][hapmap]
rs7833945	0.81[CHB][hapmap]
rs7838341	0.84[YRI][hapmap]
rs7840785	0.93[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs7841093	0.90[ASN][1000 genomes]
rs7846449	0.82[CHB][hapmap]
rs9644730	1.00[YRI][hapmap]
rs9657541	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS 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 miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv508497	chr8:10680621-10750255	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10698000-10702400	Weak transcription	Liver	Liver
2	chr8:10698000-10707800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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