Variant report

Variant	rs4679614
Chromosome Location	chr3:59810867-59810868
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:59810076..59812679-chr3:59815097..59816735,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1021227	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10428174	1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1084008	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs1485725	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1485732	1.00[ASN][1000 genomes]
rs17493	0.81[CEU][hapmap];0.89[GIH][hapmap]
rs1872495	0.93[CEU][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2605434	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2629885	0.98[EUR][1000 genomes]
rs4375999	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4679615	0.93[CEU][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs587775	0.83[EUR][1000 genomes]
rs598678	0.93[CEU][hapmap];0.87[EUR][1000 genomes]
rs608582	0.82[EUR][1000 genomes]
rs621666	0.95[GIH][hapmap]
rs6446083	1.00[ASN][1000 genomes]
rs650247	0.82[EUR][1000 genomes]
rs662910	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs6793899	1.00[ASN][1000 genomes]
rs684753	0.93[CEU][hapmap];0.89[GIH][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs687342	0.95[GIH][hapmap]
rs72888521	1.00[ASN][1000 genomes]
rs72888522	1.00[ASN][1000 genomes]
rs744192	1.00[JPT][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs936823	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014601	chr3:59666609-59888166	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv1003387	chr3:59756364-59831340	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv460562	chr3:59760118-59826778	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv590381	chr3:59760118-59826778	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv460563	chr3:59772342-59827390	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv590383	chr3:59772342-59827390	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv876837	chr3:59800539-59842644	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59770400-59825200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr3:59778200-59811200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr3:59802600-59811800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr3:59802800-59811800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr3:59802800-59821200	Weak transcription	Primary T cells from cord blood	blood
6	chr3:59807400-59816600	Weak transcription	Dnd41	blood
7	chr3:59809800-59811600	Enhancers	Fetal Thymus	thymus
8	chr3:59810400-59811000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:59810600-59811000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:59810600-59811200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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