Variant report

Variant	rs6747618
Chromosome Location	chr2:113710353-113710354
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:113703635..113705801-chr2:113709955..113711603,2	K562	blood:
2	chr2:113703635..113706262-chr2:113709716..113711603,3	K562	blood:
3	chr2:113709976..113711940-chr2:113817278..113820244,2	K562	blood:

Variant related genes	Relation type
ENSG00000136695	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10178396	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10188477	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10188765	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10199311	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10206205	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10221977	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10864907	0.92[CEU][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10864908	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123153	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123154	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11674086	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11683383	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11690399	0.85[CEU][hapmap];0.90[GIH][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11695077	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11893071	0.92[ASN][1000 genomes]
rs11897907	0.85[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12468164	0.99[ASN][1000 genomes]
rs12471839	0.92[ASN][1000 genomes]
rs12617864	0.92[ASN][1000 genomes]
rs12711745	0.98[ASN][1000 genomes]
rs12987491	0.88[ASN][1000 genomes]
rs13029531	0.85[CEU][hapmap];0.90[GIH][hapmap];0.83[MEX][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13029703	0.83[CEU][hapmap];0.81[CHB][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2068777	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2708931	0.86[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs2708932	0.88[ASN][1000 genomes]
rs2723163	0.95[CHB][hapmap];0.98[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4077216	0.91[ASN][1000 genomes]
rs4254516	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4387792	0.82[ASN][1000 genomes]
rs4538207	0.98[ASN][1000 genomes]
rs4848309	0.82[ASN][1000 genomes]
rs6716380	0.92[ASN][1000 genomes]
rs6723582	0.92[ASN][1000 genomes]
rs6735589	0.92[ASN][1000 genomes]
rs7557537	0.98[ASN][1000 genomes]
rs7559466	0.81[CEU][hapmap];0.80[JPT][hapmap]
rs879710	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs879711	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532471	chr2:113682449-113862981	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113703000-113711400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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