Variant report

Variant	rs10440631
Chromosome Location	chr5:29262646-29262647
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10044016	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10044024	0.97[ASN][1000 genomes]
rs10050443	0.97[ASN][1000 genomes]
rs10054250	0.99[ASN][1000 genomes]
rs10062606	0.99[ASN][1000 genomes]
rs10069328	0.99[ASN][1000 genomes]
rs10069894	0.99[ASN][1000 genomes]
rs10073570	0.99[ASN][1000 genomes]
rs10440642	0.98[ASN][1000 genomes]
rs10454837	0.97[ASN][1000 genomes]
rs10454851	0.97[ASN][1000 genomes]
rs10940787	0.97[ASN][1000 genomes]
rs10940788	0.97[ASN][1000 genomes]
rs10940790	0.97[ASN][1000 genomes]
rs11959636	0.98[ASN][1000 genomes]
rs13163013	0.85[ASN][1000 genomes]
rs4273618	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4317332	0.98[ASN][1000 genomes]
rs4331913	0.98[ASN][1000 genomes]
rs4346778	0.98[ASN][1000 genomes]
rs4351155	0.98[ASN][1000 genomes]
rs4370285	0.96[ASN][1000 genomes]
rs4370286	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4370287	0.99[ASN][1000 genomes]
rs4467718	0.99[ASN][1000 genomes]
rs4476737	0.99[ASN][1000 genomes]
rs4577702	0.99[ASN][1000 genomes]
rs4593279	0.95[ASN][1000 genomes]
rs4620035	0.99[ASN][1000 genomes]
rs4632809	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4632810	0.97[ASN][1000 genomes]
rs5023619	0.99[ASN][1000 genomes]
rs55891773	0.97[ASN][1000 genomes]
rs55893778	0.96[ASN][1000 genomes]
rs56009220	0.94[ASN][1000 genomes]
rs56009779	0.93[ASN][1000 genomes]
rs56104054	0.97[ASN][1000 genomes]
rs56171187	0.97[ASN][1000 genomes]
rs56252458	0.97[ASN][1000 genomes]
rs56359525	0.97[ASN][1000 genomes]
rs56403354	0.97[ASN][1000 genomes]
rs59639762	0.97[ASN][1000 genomes]
rs6450678	0.98[ASN][1000 genomes]
rs6450679	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6450680	0.97[ASN][1000 genomes]
rs66793982	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6862626	0.97[ASN][1000 genomes]
rs6881646	0.97[ASN][1000 genomes]
rs72743470	0.97[ASN][1000 genomes]
rs72743471	0.97[ASN][1000 genomes]
rs72743472	0.97[ASN][1000 genomes]
rs72743475	0.90[ASN][1000 genomes]
rs72743476	0.97[ASN][1000 genomes]
rs72743478	0.97[ASN][1000 genomes]
rs72743484	0.94[ASN][1000 genomes]
rs7341031	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7701380	0.97[ASN][1000 genomes]
rs7717789	0.97[ASN][1000 genomes]
rs7732794	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3528360	chr5:29069255-29548659	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv3528361	chr5:29069255-29548659	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1016603	chr5:29102713-29843965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv537712	chr5:29102713-29843965	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1031329	chr5:29177677-29760923	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv537713	chr5:29177677-29760923	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv880414	chr5:29194872-29495564	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv881552	chr5:29219030-29466930	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1024756	chr5:29220387-29501672	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv880722	chr5:29249544-29466930	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv968157	chr5:29252358-29348040	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
12	nsv462083	chr5:29254574-29327911	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv597752	chr5:29254574-29327911	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29262200-29263000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:29262600-29263000	Flanking Active TSS	Hela-S3	cervix
3	chr5:29262600-29263400	Active TSS	A549	lung

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