Variant report

Variant	rs56328886
Chromosome Location	chr14:39453525-39453526
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr14:39453506-39453590	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
ENSG00000199285	TF binding region

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

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs17092037	0.88[AFR][1000 genomes]
rs17108815	0.81[EUR][1000 genomes]
rs45469295	0.80[EUR][1000 genomes]
rs45469795	0.89[EUR][1000 genomes]
rs45540035	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55790340	0.89[EUR][1000 genomes]
rs55880223	0.80[EUR][1000 genomes]
rs55981737	0.80[EUR][1000 genomes]
rs55987939	0.80[EUR][1000 genomes]
rs55997577	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56063785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56074634	0.89[EUR][1000 genomes]
rs56087094	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56103446	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56125789	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56136756	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56225465	0.82[EUR][1000 genomes]
rs56237815	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56276842	0.80[EUR][1000 genomes]
rs56282196	0.80[EUR][1000 genomes]
rs56333870	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56334607	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56335002	0.89[EUR][1000 genomes]
rs56341545	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56404404	0.80[EUR][1000 genomes]
rs59418195	0.85[EUR][1000 genomes]
rs67808375	0.89[EUR][1000 genomes]
rs7147914	0.80[EUR][1000 genomes]
rs7150638	0.81[EUR][1000 genomes]
rs72669383	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72669388	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72669397	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72669399	0.80[EUR][1000 genomes]
rs72669400	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671304	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72671307	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671309	0.87[EUR][1000 genomes]
rs72671311	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671316	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671321	0.97[AFR][1000 genomes]
rs72671322	0.92[AFR][1000 genomes]
rs72671323	0.92[AFR][1000 genomes]
rs72671332	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671333	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671344	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671349	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671353	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671360	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671362	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671367	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671372	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671379	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671382	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671387	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671398	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72671400	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72673307	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72673314	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72673315	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72673316	0.89[EUR][1000 genomes]
rs72673317	0.89[EUR][1000 genomes]
rs72673318	0.87[EUR][1000 genomes]
rs72673328	0.85[EUR][1000 genomes]
rs72673329	0.85[EUR][1000 genomes]
rs72673339	0.85[EUR][1000 genomes]
rs72673346	0.80[EUR][1000 genomes]
rs72673350	0.80[EUR][1000 genomes]
rs8009457	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	esv3429206	chr14:39160730-39648836	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv901657	chr14:39410706-39460072	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1038622	chr14:39423562-39604035	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv564417	chr14:39452317-39535560	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39450000-39465000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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