Variant report

Variant	rs6507469
Chromosome Location	chr18:39867904-39867905
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1026595	0.92[ASN][1000 genomes]
rs1026596	0.92[ASN][1000 genomes]
rs10502780	0.85[ASN][1000 genomes]
rs11082268	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12455999	0.91[EUR][1000 genomes]
rs12457855	0.92[ASN][1000 genomes]
rs12457879	0.92[ASN][1000 genomes]
rs12457881	0.92[ASN][1000 genomes]
rs12605925	0.92[ASN][1000 genomes]
rs12956046	0.92[ASN][1000 genomes]
rs12967041	0.92[ASN][1000 genomes]
rs12967873	0.92[ASN][1000 genomes]
rs1381349	0.85[ASN][1000 genomes]
rs1461715	0.92[ASN][1000 genomes]
rs1461717	0.92[ASN][1000 genomes]
rs1461718	0.86[ASN][1000 genomes]
rs1461719	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1461721	0.85[ASN][1000 genomes]
rs1461723	0.87[EUR][1000 genomes]
rs1599478	0.84[EUR][1000 genomes]
rs1870781	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1870782	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1870783	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1870785	0.92[ASN][1000 genomes]
rs2219638	0.85[ASN][1000 genomes]
rs2335779	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34703522	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35073620	0.85[ASN][1000 genomes]
rs35959504	0.85[ASN][1000 genomes]
rs4890391	0.92[ASN][1000 genomes]
rs4890393	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4890394	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4890395	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62082201	0.85[ASN][1000 genomes]
rs7228003	0.85[EUR][1000 genomes]
rs7235905	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7236024	0.85[ASN][1000 genomes]
rs7238496	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7241462	0.92[ASN][1000 genomes]
rs8085350	0.92[ASN][1000 genomes]
rs8085753	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8089080	0.93[EUR][1000 genomes]
rs8089100	1.00[ASN][1000 genomes]
rs882289	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs882290	0.92[ASN][1000 genomes]
rs882291	0.92[ASN][1000 genomes]
rs898785	0.92[ASN][1000 genomes]
rs898786	0.92[ASN][1000 genomes]
rs898790	0.92[ASN][1000 genomes]
rs898791	0.92[ASN][1000 genomes]
rs898792	0.92[ASN][1000 genomes]
rs898793	0.92[ASN][1000 genomes]
rs898794	0.92[ASN][1000 genomes]
rs9304268	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	esv34153	chr18:39398768-39872265	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1059409	chr18:39711099-40139446	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1063343	chr18:39760943-39898498	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
5	nsv1059553	chr18:39828781-39872695	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39866400-39868600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr18:39867200-39868000	Enhancers	Brain Substantia Nigra	brain
3	chr18:39867200-39868400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr18:39867800-39868200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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