Variant report

Variant	rs586283
Chromosome Location	chr2:111949561-111949562
allele	C/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	FOXA2	chr2:111949388-111949625	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:111949295..111952231-chr2:111957401..111960814,4	K562	blood:
2	chr2:111949350..111952010-chr2:111953773..111956343,2	K562	blood:

Variant related genes	Relation type
ENSG00000230499	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10166773	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10169613	0.80[EUR][1000 genomes]
rs10199020	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10439381	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10439396	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13398360	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28723045	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3898882	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55878194	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60982612	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6542350	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6732491	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6754738	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6755484	0.80[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs744530	0.81[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs7562480	0.81[EUR][1000 genomes]
rs7565445	0.81[EUR][1000 genomes]
rs7565457	0.81[EUR][1000 genomes]
rs7565473	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7569300	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7572367	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7581735	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7585054	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7588534	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs879623	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9308742	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs938095	0.92[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9808225	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv834331	chr2:111812139-112004678	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	esv1803356	chr2:111899783-112662597	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv428402	chr2:111899783-112662597	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1801950	chr2:111899783-112746937	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	esv2757825	chr2:111899783-112746937	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	esv2759083	chr2:111899783-112746937	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111944400-111957400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:111944600-111950200	Weak transcription	Stomach Mucosa	stomach
3	chr2:111945000-111952000	Weak transcription	Fetal Intestine Large	intestine
4	chr2:111948800-111950000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:111948800-111950800	Enhancers	HepG2	liver
6	chr2:111949000-111950000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:111949400-111951800	Weak transcription	GM12878-XiMat	blood

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