Variant report

Variant	rs59559279
Chromosome Location	chr4:90799072-90799073
allele	C/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	chr4:90799052-90799221	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
MMRN1	TF binding region

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10433954	0.87[ASN][1000 genomes]
rs10433955	0.87[ASN][1000 genomes]
rs10516850	0.85[ASN][1000 genomes]
rs10516851	0.85[ASN][1000 genomes]
rs10516852	0.85[ASN][1000 genomes]
rs11722543	0.98[ASN][1000 genomes]
rs12640573	0.85[ASN][1000 genomes]
rs12640925	0.87[ASN][1000 genomes]
rs12640973	0.87[ASN][1000 genomes]
rs12641781	0.85[ASN][1000 genomes]
rs12643790	0.84[ASN][1000 genomes]
rs12643823	0.85[ASN][1000 genomes]
rs12644375	0.85[ASN][1000 genomes]
rs1372511	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1372512	0.98[ASN][1000 genomes]
rs1442131	0.88[ASN][1000 genomes]
rs1442132	0.98[ASN][1000 genomes]
rs17016373	0.87[ASN][1000 genomes]
rs2241884	0.85[ASN][1000 genomes]
rs3775464	0.87[ASN][1000 genomes]
rs3775465	0.87[ASN][1000 genomes]
rs3775466	0.87[ASN][1000 genomes]
rs3775467	0.87[ASN][1000 genomes]
rs3775473	0.84[ASN][1000 genomes]
rs3775474	0.85[ASN][1000 genomes]
rs3775476	0.85[ASN][1000 genomes]
rs3775477	0.85[ASN][1000 genomes]
rs3775478	0.85[ASN][1000 genomes]
rs56146644	0.87[ASN][1000 genomes]
rs57925841	0.98[ASN][1000 genomes]
rs58514521	0.87[ASN][1000 genomes]
rs58930449	0.81[ASN][1000 genomes]
rs60341854	0.84[ASN][1000 genomes]
rs60847430	0.87[ASN][1000 genomes]
rs61160271	0.85[ASN][1000 genomes]
rs61611959	0.81[ASN][1000 genomes]
rs6532197	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6532199	0.98[ASN][1000 genomes]
rs6532200	0.90[ASN][1000 genomes]
rs6828095	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6838943	0.88[ASN][1000 genomes]
rs6847403	0.98[ASN][1000 genomes]
rs6848022	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6857668	0.83[ASN][1000 genomes]
rs6858182	0.85[ASN][1000 genomes]
rs72657800	0.88[ASN][1000 genomes]
rs72657801	0.87[ASN][1000 genomes]
rs72657802	0.87[ASN][1000 genomes]
rs72659403	0.87[ASN][1000 genomes]
rs72659404	0.87[ASN][1000 genomes]
rs72659409	0.85[ASN][1000 genomes]
rs72659413	0.81[ASN][1000 genomes]
rs73831836	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73831856	0.83[ASN][1000 genomes]
rs7657014	0.92[ASN][1000 genomes]
rs7666981	0.87[ASN][1000 genomes]
rs7673735	0.98[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	nsv997700	chr4:90791866-90920021	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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