Variant report

Variant	rs72735955
Chromosome Location	chr14:72463283-72463284
allele	A/G
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	chr14:72463282-72463566	HepG2	liver:	n/a	n/a
2	MAFK	chr14:72463259-72463589	HepG2	liver:	n/a	n/a
3	MAFF	chr14:72463280-72463500	HepG2	liver:	n/a	chr14:72463409-72463427
4	MAFK	chr14:72463277-72463497	IMR90	lung:	n/a	n/a

Variant related genes	Relation type
ENSG00000257040	TF binding region

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1009017	0.96[ASN][1000 genomes]
rs11158920	0.84[EUR][1000 genomes]
rs11158926	0.86[ASN][1000 genomes]
rs11158927	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11620690	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11622507	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11623492	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11623535	0.95[ASN][1000 genomes]
rs11625937	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11627768	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11628133	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11628574	0.87[EUR][1000 genomes]
rs12148043	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1476745	0.86[ASN][1000 genomes]
rs17093750	0.84[EUR][1000 genomes]
rs17104493	0.81[EUR][1000 genomes]
rs17105346	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17105566	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17105606	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17768361	0.86[ASN][1000 genomes]
rs1987722	0.97[ASN][1000 genomes]
rs1987723	0.96[ASN][1000 genomes]
rs2010846	0.97[ASN][1000 genomes]
rs2010850	0.97[ASN][1000 genomes]
rs2052015	0.86[EUR][1000 genomes]
rs2238277	0.86[EUR][1000 genomes]
rs2332705	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3784055	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3784056	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4243640	0.97[ASN][1000 genomes]
rs4350510	0.99[ASN][1000 genomes]
rs4354860	0.97[ASN][1000 genomes]
rs4899409	0.85[EUR][1000 genomes]
rs4902958	0.85[EUR][1000 genomes]
rs4902966	0.97[ASN][1000 genomes]
rs56743778	0.84[EUR][1000 genomes]
rs58890880	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59631889	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60503142	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs699358	0.97[ASN][1000 genomes]
rs72734102	0.83[EUR][1000 genomes]
rs72735921	0.84[EUR][1000 genomes]
rs72735923	0.84[EUR][1000 genomes]
rs72735952	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72735956	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7493353	0.82[EUR][1000 genomes]
rs7494103	0.87[EUR][1000 genomes]
rs8013467	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 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	chr14:72462600-72465200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72462800-72463600	Weak transcription	Left Ventricle	heart
3	chr14:72462800-72467200	Weak transcription	Right Ventricle	heart
4	chr14:72463000-72463400	Enhancers	Cortex derived primary cultured neurospheres	brain

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