Variant report

Variant	rs4682447
Chromosome Location	chr3:112662937-112662938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1016348	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs12497951	0.82[ASN][1000 genomes]
rs1387023	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1392786	0.91[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1466872	0.81[ASN][1000 genomes]
rs1488193	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1844084	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2087284	0.91[CHB][hapmap]
rs2171509	0.81[ASN][1000 genomes]
rs4103791	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs4234417	0.91[CHB][hapmap]
rs4682125	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs4682441	0.89[CHB][hapmap]
rs6438118	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs6438119	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs6438120	0.91[CHB][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs6438122	0.91[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs6769091	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs6772799	0.81[ASN][1000 genomes]
rs6784838	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs6808249	0.91[CHB][hapmap]
rs7355890	0.80[ASN][1000 genomes]
rs7611690	0.81[ASN][1000 genomes]
rs7615462	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs7615572	0.87[CHB][hapmap]
rs7622812	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs7622814	0.91[CHB][hapmap]
rs7640561	0.86[CHB][hapmap]
rs7646849	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs7652504	0.81[ASN][1000 genomes]
rs9815606	0.81[ASN][1000 genomes]
rs9823363	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs9826308	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs9833991	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs9834353	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs9834840	0.82[ASN][1000 genomes]
rs9847365	0.91[CHB][hapmap]
rs9854885	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs9864295	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs9865242	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs9868053	0.81[ASN][1000 genomes]
rs9870335	0.82[ASN][1000 genomes]
rs9870568	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs9871985	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs9877631	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	esv1843165	chr3:112628205-112740145	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112660800-112663400	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr3:112661000-112663400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr3:112661000-112665400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr3:112661000-112669800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr3:112661200-112677000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr3:112662000-112667800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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