Variant report

Variant	rs10433953
Chromosome Location	chr4:90698964-90698965
allele	G/T
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:70)

rs_ID	r²[population]
rs10003708	0.81[ASN][1000 genomes]
rs10025915	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10033209	0.82[ASN][1000 genomes]
rs1045722	0.82[ASN][1000 genomes]
rs10516845	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11931062	0.99[ASN][1000 genomes]
rs11935469	0.99[ASN][1000 genomes]
rs11944331	0.99[ASN][1000 genomes]
rs11945223	0.81[ASN][1000 genomes]
rs12640100	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12642514	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12648141	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17016071	0.82[ASN][1000 genomes]
rs17016168	1.00[AFR][1000 genomes]
rs17016255	0.87[AFR][1000 genomes]
rs2035268	0.92[AFR][1000 genomes]
rs2737029	0.99[ASN][1000 genomes]
rs28393675	0.81[ASN][1000 genomes]
rs28412513	0.82[ASN][1000 genomes]
rs28613708	0.81[ASN][1000 genomes]
rs28781297	0.99[ASN][1000 genomes]
rs34699553	0.92[AFR][1000 genomes]
rs35495602	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs35541731	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs356165	0.82[ASN][1000 genomes]
rs356203	0.82[ASN][1000 genomes]
rs3756054	0.82[ASN][1000 genomes]
rs3775422	0.81[ASN][1000 genomes]
rs3775423	0.82[ASN][1000 genomes]
rs3775424	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3775427	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3775433	0.99[ASN][1000 genomes]
rs3775434	0.99[ASN][1000 genomes]
rs3775439	0.99[ASN][1000 genomes]
rs3775458	0.93[AFR][1000 genomes]
rs3796661	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3822086	0.82[ASN][1000 genomes]
rs3822089	0.99[ASN][1000 genomes]
rs3822090	0.99[ASN][1000 genomes]
rs3857049	0.89[EUR][1000 genomes]
rs3857051	0.81[ASN][1000 genomes]
rs3857052	0.81[ASN][1000 genomes]
rs3857053	0.82[ASN][1000 genomes]
rs3857057	0.82[ASN][1000 genomes]
rs3857058	0.82[ASN][1000 genomes]
rs3857059	0.82[ASN][1000 genomes]
rs3857061	0.99[ASN][1000 genomes]
rs3899608	0.99[ASN][1000 genomes]
rs3906824	0.89[AFR][1000 genomes]
rs4031753	0.99[ASN][1000 genomes]
rs4088093	0.82[ASN][1000 genomes]
rs4088094	0.82[ASN][1000 genomes]
rs4122861	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58054215	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs60031383	0.99[ASN][1000 genomes]
rs60642683	0.88[AFR][1000 genomes]
rs61032876	0.81[ASN][1000 genomes]
rs6822088	0.92[ASN][1000 genomes]
rs6826785	0.98[ASN][1000 genomes]
rs6834765	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7436973	0.81[ASN][1000 genomes]
rs7655611	0.99[ASN][1000 genomes]
rs7655792	0.81[ASN][1000 genomes]
rs7661330	0.82[ASN][1000 genomes]
rs7675290	0.82[ASN][1000 genomes]
rs7684318	0.82[ASN][1000 genomes]
rs7690873	0.99[ASN][1000 genomes]
rs7698672	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs8180209	0.82[ASN][1000 genomes]
rs8180214	0.81[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	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv879536	chr4:90678541-90775212	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90676200-90709200	Weak transcription	HUVEC	blood vessel
2	chr4:90687200-90718400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:90688800-90704800	Weak transcription	Fetal Lung	lung
4	chr4:90691800-90704800	Weak transcription	Brain Angular Gyrus	brain
5	chr4:90693000-90709400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:90696200-90699000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:90697000-90711000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:90697400-90702800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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