Variant report

Variant	rs34592526
Chromosome Location	chr6:88116036-88116037
allele	A/C
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	POLR2A	chr6:88115357-88116146	K562	blood:	n/a	n/a
2	NFYB	chr6:88115979-88116217	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
C6orf165	TF binding region
ENSG00000272514	TF binding region

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs12178951	0.89[EUR][1000 genomes]
rs12529618	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12529631	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12530034	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13192579	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13195057	0.82[EUR][1000 genomes]
rs13197065	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13198605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13205397	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13217556	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13217637	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13218502	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13219364	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13220737	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16879293	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16879295	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2875534	0.96[EUR][1000 genomes]
rs34144911	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34294674	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34373986	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34726630	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34914404	0.96[EUR][1000 genomes]
rs35243146	1.00[AMR][1000 genomes]
rs35562204	0.93[EUR][1000 genomes]
rs35580717	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35756344	0.96[EUR][1000 genomes]
rs35822597	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs45563737	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58735049	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs60711734	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6454604	0.96[EUR][1000 genomes]
rs66632635	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs66786089	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs66805147	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs66819255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67569613	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67776922	0.96[EUR][1000 genomes]
rs68100217	0.89[EUR][1000 genomes]
rs71572754	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71572755	0.96[EUR][1000 genomes]
rs71572757	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71572758	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71572762	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	nsv1018155	chr6:88049729-88272862	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv830722	chr6:88054186-88223625	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1031961	chr6:88110401-88367006	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88040600-88116800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:88106400-88117200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:88106400-88117200	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:88107200-88117000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:88108000-88117000	Weak transcription	Brain Inferior Temporal Lobe	brain

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