Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10000005	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11099638	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11736000	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11945980	0.99[ASN][1000 genomes]
rs12506772	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1495143	0.92[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs1495147	0.98[ASN][1000 genomes]
rs1532357	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1532358	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17363778	0.84[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs2201487	0.99[ASN][1000 genomes]
rs2220887	0.88[ASN][1000 genomes]
rs28462176	0.99[ASN][1000 genomes]
rs28857537	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs348702	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs348704	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5023577	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7657139	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7686616	0.96[CEU][hapmap];0.83[CHB][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs903521	1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap];0.86[LWK][hapmap];0.86[MEX][hapmap];0.89[YRI][hapmap];0.93[ASN][1000 genomes]
rs903522	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524354	chr4:85006975-85215142	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv829996	chr4:85016673-85173300	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv879514	chr4:85057124-85272572	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1012379	chr4:85071268-85205732	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85145400-85152600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:85151200-85154400	Enhancers	Fetal Lung	lung
3	chr4:85151400-85152800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:85152200-85152600	Weak transcription	Fetal Stomach	stomach

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