Variant report

Variant	rs11167711
Chromosome Location	chr5:154495085-154495086
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	MAFF	chr5:154494898-154495090	HepG2	liver:	n/a	chr5:154494914-154494932
2	NFYB	chr5:154495048-154495461	K562	blood:	n/a	n/a
3	SP1	chr5:154494954-154495316	GM12878	blood:	n/a	n/a
4	SP1	chr5:154495065-154495385	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000253646	TF binding region

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10039301	0.86[ASN][1000 genomes]
rs10042611	0.86[ASN][1000 genomes]
rs10223164	0.95[ASN][1000 genomes]
rs1026974	0.86[ASN][1000 genomes]
rs11167708	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11167709	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12153378	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12153386	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12187210	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12188764	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12188773	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12513733	0.86[ASN][1000 genomes]
rs12517423	0.86[ASN][1000 genomes]
rs12519670	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12519696	0.86[ASN][1000 genomes]
rs28482784	0.86[ASN][1000 genomes]
rs34021636	0.83[EUR][1000 genomes]
rs34121599	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35025199	0.86[ASN][1000 genomes]
rs35235180	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4958396	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4958776	0.95[ASN][1000 genomes]
rs4958780	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6868742	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6868904	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6890088	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6890098	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6898774	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9324802	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883059	chr5:154457905-154556230	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv462492	chr5:154489393-154523910	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv600091	chr5:154489393-154523910	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr5:154492200-154495800	Weak transcription	Placenta Amnion	Placenta Amnion

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