Variant report

Variant	rs62568692
Chromosome Location	chr9:79040538-79040539
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10116800	1.00[ASN][1000 genomes]
rs10118954	1.00[ASN][1000 genomes]
rs10119732	0.95[ASN][1000 genomes]
rs10125012	1.00[ASN][1000 genomes]
rs10125667	1.00[ASN][1000 genomes]
rs10781358	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10781359	0.95[ASN][1000 genomes]
rs10781360	1.00[ASN][1000 genomes]
rs10869770	1.00[ASN][1000 genomes]
rs10869774	0.95[ASN][1000 genomes]
rs10869781	0.84[EUR][1000 genomes]
rs11144870	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11144875	1.00[ASN][1000 genomes]
rs11144878	1.00[ASN][1000 genomes]
rs11144881	1.00[ASN][1000 genomes]
rs11144887	1.00[ASN][1000 genomes]
rs11144894	0.95[ASN][1000 genomes]
rs11144897	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11144908	0.91[EUR][1000 genomes]
rs11144909	0.91[EUR][1000 genomes]
rs1129399	1.00[ASN][1000 genomes]
rs11548954	0.89[ASN][1000 genomes]
rs11548955	0.91[AMR][1000 genomes]
rs11791951	1.00[ASN][1000 genomes]
rs11793613	1.00[ASN][1000 genomes]
rs11794019	1.00[ASN][1000 genomes]
rs12156473	1.00[ASN][1000 genomes]
rs12375735	0.83[ASN][1000 genomes]
rs12377856	1.00[ASN][1000 genomes]
rs12377878	1.00[ASN][1000 genomes]
rs12380332	0.84[ASN][1000 genomes]
rs12380522	0.90[ASN][1000 genomes]
rs1324213	1.00[ASN][1000 genomes]
rs1951910	1.00[ASN][1000 genomes]
rs3187236	0.90[ASN][1000 genomes]
rs4571791	1.00[ASN][1000 genomes]
rs55740812	0.94[ASN][1000 genomes]
rs57339182	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57480680	1.00[ASN][1000 genomes]
rs58136435	0.95[ASN][1000 genomes]
rs59424752	0.90[ASN][1000 genomes]
rs62564441	0.90[ASN][1000 genomes]
rs62564442	0.90[ASN][1000 genomes]
rs62564446	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62564449	0.91[EUR][1000 genomes]
rs62564454	0.90[EUR][1000 genomes]
rs62565109	0.83[ASN][1000 genomes]
rs62567918	0.94[ASN][1000 genomes]
rs62567919	0.89[ASN][1000 genomes]
rs62568690	1.00[ASN][1000 genomes]
rs6560516	1.00[ASN][1000 genomes]
rs7023191	0.90[ASN][1000 genomes]
rs7025942	1.00[ASN][1000 genomes]
rs7026067	1.00[ASN][1000 genomes]
rs7029439	1.00[ASN][1000 genomes]
rs7035385	1.00[ASN][1000 genomes]
rs7037345	0.90[ASN][1000 genomes]
rs7038009	1.00[ASN][1000 genomes]
rs7038056	0.90[ASN][1000 genomes]
rs7040138	1.00[ASN][1000 genomes]
rs7041690	1.00[ASN][1000 genomes]
rs7047489	1.00[ASN][1000 genomes]
rs7049245	1.00[ASN][1000 genomes]
rs7851616	1.00[ASN][1000 genomes]
rs7852884	1.00[ASN][1000 genomes]
rs7853410	1.00[ASN][1000 genomes]
rs7854540	0.84[ASN][1000 genomes]
rs7859327	1.00[ASN][1000 genomes]
rs7875575	1.00[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	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv931033	chr9:78850330-79366454	Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893478	chr9:78933874-79101006	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv893479	chr9:78971253-79275226	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv3451027	chr9:79021447-79056132	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 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	chr9:79034800-79046000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:79038000-79046800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:79039400-79041400	Enhancers	HepG2	liver

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