Variant report

Variant	rs11694118
Chromosome Location	chr2:208941724-208941725
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:208913270..208916048-chr2:208940472..208942742,2	MCF-7	breast:
2	chr2:208935178..208937154-chr2:208940190..208941817,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10932231	0.89[ASN][1000 genomes]
rs10932232	0.88[ASN][1000 genomes]
rs10932233	0.89[ASN][1000 genomes]
rs10932237	0.85[ASN][1000 genomes]
rs10932238	0.98[ASN][1000 genomes]
rs11681747	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11683477	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11892539	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11892554	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11894673	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11896152	0.90[ASN][1000 genomes]
rs11896248	0.90[ASN][1000 genomes]
rs12465847	0.94[ASN][1000 genomes]
rs12987978	0.90[ASN][1000 genomes]
rs16840404	0.90[ASN][1000 genomes]
rs17538082	0.85[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2123296	0.98[ASN][1000 genomes]
rs34100088	0.90[ASN][1000 genomes]
rs35306034	0.90[ASN][1000 genomes]
rs4234085	0.85[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4287753	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4673378	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4675729	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4675730	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4675731	0.98[ASN][1000 genomes]
rs62192797	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6711974	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6723206	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6727089	0.85[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6727122	0.90[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6735060	0.98[ASN][1000 genomes]
rs6746998	0.89[ASN][1000 genomes]
rs7422654	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7422655	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs896637	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv2760541	chr2:208936949-208945639	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	1 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	chr2:208941400-208942000	Enhancers	Placenta	Placenta
2	chr2:208941600-208942800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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