Variant report

Variant	rs263668
Chromosome Location	chr2:211093153-211093154
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	CTCF	chr2:211093139-211093213	GM10248	blood:	n/a	n/a

Variant related genes	Relation type
ACADL	TF binding region

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10179268	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10192315	1.00[ASN][1000 genomes]
rs1155845	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11675027	1.00[ASN][1000 genomes]
rs11678206	1.00[ASN][1000 genomes]
rs11682370	1.00[ASN][1000 genomes]
rs11686587	1.00[ASN][1000 genomes]
rs11688180	1.00[ASN][1000 genomes]
rs11688922	1.00[ASN][1000 genomes]
rs11900095	0.80[EUR][1000 genomes]
rs12989455	1.00[ASN][1000 genomes]
rs12992714	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13002602	1.00[ASN][1000 genomes]
rs13006132	1.00[ASN][1000 genomes]
rs13009071	1.00[ASN][1000 genomes]
rs13009890	1.00[ASN][1000 genomes]
rs13011543	1.00[ASN][1000 genomes]
rs13015354	1.00[ASN][1000 genomes]
rs13015487	0.80[EUR][1000 genomes]
rs13017647	1.00[ASN][1000 genomes]
rs13017752	1.00[ASN][1000 genomes]
rs13018349	1.00[ASN][1000 genomes]
rs13019613	1.00[ASN][1000 genomes]
rs13020232	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13021055	1.00[ASN][1000 genomes]
rs13022638	0.80[EUR][1000 genomes]
rs13023313	0.80[EUR][1000 genomes]
rs13025700	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13415601	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509568	0.96[EUR][1000 genomes]
rs1509570	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509571	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509572	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16844058	1.00[ASN][1000 genomes]
rs16844213	0.98[EUR][1000 genomes]
rs2048277	0.80[EUR][1000 genomes]
rs2160020	1.00[ASN][1000 genomes]
rs2539005	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs263675	1.00[ASN][1000 genomes]
rs263680	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs263681	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs263686	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34334556	1.00[ASN][1000 genomes]
rs34678259	1.00[ASN][1000 genomes]
rs34693593	0.80[EUR][1000 genomes]
rs35125543	1.00[ASN][1000 genomes]
rs36080651	1.00[ASN][1000 genomes]
rs62202972	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6435561	1.00[ASN][1000 genomes]
rs6714161	1.00[ASN][1000 genomes]
rs6716836	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6732072	1.00[ASN][1000 genomes]
rs6732486	1.00[ASN][1000 genomes]
rs6732506	1.00[ASN][1000 genomes]
rs6735292	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6749996	0.80[EUR][1000 genomes]
rs6754591	1.00[ASN][1000 genomes]
rs6760874	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71350736	1.00[ASN][1000 genomes]
rs71350737	0.80[EUR][1000 genomes]
rs7557043	1.00[ASN][1000 genomes]
rs7609345	1.00[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	esv1795338	chr2:210758078-211098113	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv1802749	chr2:210905194-211255611	Strong transcription ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	esv1803710	chr2:211073376-211173763	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1012567	chr2:211087588-211315554	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211090400-211094400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:211090400-211095400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:211090600-211095000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:211090800-211095000	Weak transcription	Placenta	Placenta
5	chr2:211091000-211099800	Weak transcription	Aorta	Aorta
6	chr2:211091200-211096800	Enhancers	Liver	Liver
7	chr2:211092400-211094000	Enhancers	Pancreas	Pancrea
8	chr2:211092800-211100200	Weak transcription	Gastric	stomach

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