Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11769082	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11769090	0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11971318	0.84[AMR][1000 genomes]
rs11974825	0.84[AMR][1000 genomes]
rs12535207	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12537571	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1624657	0.80[ASN][1000 genomes]
rs1689296	0.80[ASN][1000 genomes]
rs1689297	0.80[ASN][1000 genomes]
rs1689299	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1731306	0.80[ASN][1000 genomes]
rs1731319	0.82[EUR][1000 genomes]
rs1731320	0.80[ASN][1000 genomes]
rs1919940	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2164	0.80[ASN][1000 genomes]
rs4947758	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4947759	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55780372	0.81[AMR][1000 genomes]
rs55924429	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56205304	0.84[AMR][1000 genomes]
rs56219635	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59981499	0.84[AMR][1000 genomes]
rs60794096	0.81[AMR][1000 genomes]
rs6964681	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73113344	0.80[ASN][1000 genomes]
rs7797901	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1017676	chr7:52932139-53350524	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv831001	chr7:53003534-53152783	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv607008	chr7:53009355-53068819	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases
5	nsv464449	chr7:53009493-53026365	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv607009	chr7:53009493-53026365	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53015800-53018400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:53016800-53023400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:53017200-53023400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:53017200-53026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:53017200-53026800	Weak transcription	Fetal Heart	heart

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