Variant report

Variant	rs766400
Chromosome Location	chr1:186687347-186687348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:186686366..186688397-chr1:186690358..186692052,2	MCF-7	breast:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10737269	0.91[EUR][1000 genomes]
rs10752971	0.91[EUR][1000 genomes]
rs10752973	0.91[EUR][1000 genomes]
rs10752974	0.91[EUR][1000 genomes]
rs10798055	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798057	0.91[EUR][1000 genomes]
rs10911922	0.91[EUR][1000 genomes]
rs11567835	1.00[ASN][1000 genomes]
rs11567836	1.00[ASN][1000 genomes]
rs1158042	0.91[EUR][1000 genomes]
rs1158043	0.91[EUR][1000 genomes]
rs12029765	0.91[EUR][1000 genomes]
rs12116711	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12117451	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12119919	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12124257	0.80[CEU][hapmap]
rs12144220	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12720491	1.00[ASN][1000 genomes]
rs13376484	1.00[ASN][1000 genomes]
rs16825688	1.00[JPT][hapmap]
rs1980454	0.89[EUR][1000 genomes]
rs2205951	0.91[EUR][1000 genomes]
rs2223310	1.00[JPT][hapmap]
rs2223329	0.98[EUR][1000 genomes]
rs2223330	0.98[EUR][1000 genomes]
rs4648298	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4648311	1.00[ASN][1000 genomes]
rs4650701	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4650705	1.00[JPT][hapmap]
rs59638687	1.00[ASN][1000 genomes]
rs59873426	1.00[ASN][1000 genomes]
rs6425049	0.89[EUR][1000 genomes]
rs6660635	0.87[EUR][1000 genomes]
rs6663605	0.91[EUR][1000 genomes]
rs6688484	0.91[EUR][1000 genomes]
rs6692679	0.89[EUR][1000 genomes]
rs6695425	1.00[JPT][hapmap]
rs689462	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs689469	1.00[ASN][1000 genomes]
rs689470	1.00[JPT][hapmap]
rs7418312	0.91[EUR][1000 genomes]
rs7516460	0.89[EUR][1000 genomes]
rs7523981	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7532307	0.87[EUR][1000 genomes]
rs7554410	0.89[EUR][1000 genomes]
rs7555275	0.91[EUR][1000 genomes]
rs964570	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers 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	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv2762854	chr1:186547101-186847574	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv470750	chr1:186642429-186700959	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv548403	chr1:186642429-186700959	Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv466261	chr1:186652395-186742947	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv548405	chr1:186652395-186742947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 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	chr1:186686000-186688400	Enhancers	Hela-S3	cervix
2	chr1:186686200-186687400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:186686200-186687400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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