Variant report

Variant	rs7730857
Chromosome Location	chr5:49657350-49657351
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10041033	0.83[ASN][1000 genomes]
rs10042504	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10055539	0.86[ASN][1000 genomes]
rs10060219	0.81[AMR][1000 genomes]
rs10061339	0.82[ASN][1000 genomes]
rs10062032	0.83[AMR][1000 genomes]
rs10071725	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10072182	0.81[EUR][1000 genomes]
rs10073530	0.81[EUR][1000 genomes]
rs10074359	0.83[AMR][1000 genomes]
rs10076490	0.87[ASN][1000 genomes]
rs10079493	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1039797	0.86[ASN][1000 genomes]
rs1039798	0.81[EUR][1000 genomes]
rs10471362	0.87[ASN][1000 genomes]
rs11959569	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12651909	0.89[ASN][1000 genomes]
rs12697055	0.83[AMR][1000 genomes]
rs13173678	0.81[ASN][1000 genomes]
rs13174293	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13180767	0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13180852	0.83[ASN][1000 genomes]
rs13185587	0.87[ASN][1000 genomes]
rs13357429	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1344339	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1511737	0.81[AMR][1000 genomes]
rs1511738	0.81[AMR][1000 genomes]
rs1606224	0.83[AMR][1000 genomes]
rs16879094	0.83[ASN][1000 genomes]
rs1812994	0.87[ASN][1000 genomes]
rs1995795	0.86[ASN][1000 genomes]
rs2036902	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2089605	0.83[ASN][1000 genomes]
rs2137132	0.86[ASN][1000 genomes]
rs2137134	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2668024	0.80[ASN][1000 genomes]
rs28528780	0.83[ASN][1000 genomes]
rs28676351	0.80[ASN][1000 genomes]
rs303235	0.86[ASN][1000 genomes]
rs303237	0.85[ASN][1000 genomes]
rs34601168	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34741488	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs34749302	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34945845	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35740733	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3849669	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3849670	0.87[ASN][1000 genomes]
rs3860732	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3950451	0.89[ASN][1000 genomes]
rs4029989	0.82[ASN][1000 genomes]
rs4030569	0.90[ASN][1000 genomes]
rs4030570	0.90[ASN][1000 genomes]
rs4030571	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4030572	0.86[ASN][1000 genomes]
rs4030573	0.89[ASN][1000 genomes]
rs4031137	0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4145844	0.81[ASN][1000 genomes]
rs4337857	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4398636	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4495185	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4549528	0.90[ASN][1000 genomes]
rs4571473	0.86[ASN][1000 genomes]
rs4637546	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4865519	0.81[AMR][1000 genomes]
rs57137858	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58756661	0.83[ASN][1000 genomes]
rs59254474	0.81[ASN][1000 genomes]
rs62365896	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62386175	0.92[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6449961	0.83[AMR][1000 genomes]
rs6450056	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6450063	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6450098	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6450099	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6450107	0.83[ASN][1000 genomes]
rs6450139	0.83[ASN][1000 genomes]
rs6863840	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6868677	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6869871	0.83[ASN][1000 genomes]
rs6871761	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6874829	0.86[ASN][1000 genomes]
rs6876902	0.83[AMR][1000 genomes]
rs6877713	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6897412	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7341010	0.83[AMR][1000 genomes]
rs7442762	0.81[EUR][1000 genomes]
rs7446360	0.83[ASN][1000 genomes]
rs7446951	0.83[AMR][1000 genomes]
rs7447926	0.81[AMR][1000 genomes]
rs7700537	0.80[AMR][1000 genomes]
rs7712849	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7717982	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7721808	0.87[ASN][1000 genomes]
rs7722742	0.83[AMR][1000 genomes]
rs7732000	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9291925	0.83[AMR][1000 genomes]
rs9292005	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019539	chr5:49455624-49702736	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1023402	chr5:49455624-49708458	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1032003	chr5:49455624-49881491	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1016583	chr5:49455624-50116720	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1023140	chr5:49455624-50121623	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1023981	chr5:49584188-49871537	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv537757	chr5:49584188-49871537	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1022067	chr5:49584188-49960083	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv537758	chr5:49584188-49960083	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv918220	chr5:49584188-50111282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv931010	chr5:49584189-50118254	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv916441	chr5:49584313-49831223	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv523212	chr5:49597497-50058043	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	nsv965616	chr5:49642415-49658734	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
15	nsv4818	chr5:49647989-49661497	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7730857	EMB	cis	Whole Blood	GTEx
rs7730857	EMB	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49649600-49659000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr5:49652600-49658800	Weak transcription	Dnd41	blood
3	chr5:49652800-49665400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr5:49653000-49658000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr5:49654200-49658600	Weak transcription	Primary B cells from cord blood	blood
6	chr5:49656400-49661800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr5:49656400-49677800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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