Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:183139290..183141946-chr2:183155474..183158091,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1070197	0.86[EUR][1000 genomes]
rs1383899	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16822918	0.81[EUR][1000 genomes]
rs16822938	0.86[EUR][1000 genomes]
rs1842640	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1967008	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2438290	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2568683	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2568684	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2568686	0.86[EUR][1000 genomes]
rs2623421	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs300888	0.86[EUR][1000 genomes]
rs711807	0.86[EUR][1000 genomes]
rs73032449	0.86[EUR][1000 genomes]
rs73036255	0.86[EUR][1000 genomes]
rs833130	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs833138	0.86[EUR][1000 genomes]
rs833139	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs833143	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs833157	0.86[EUR][1000 genomes]
rs833161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs866732	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv583913	chr2:183043563-183243313	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv533782	chr2:183059730-183500040	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1008825	chr2:183067339-183228668	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv536066	chr2:183067339-183228668	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:183149000-183158200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:183155600-183156400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:183155800-183156600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:183156000-183156600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:183156200-183156600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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