Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:78948422..78950339-chr14:78950508..78953460,2	K562	blood:

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10135111	1.00[AMR][1000 genomes]
rs10135475	1.00[AMR][1000 genomes]
rs11159360	1.00[AMR][1000 genomes]
rs1156946	1.00[AMR][1000 genomes]
rs1468744	1.00[YRI][hapmap]
rs1990530	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2052202	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2052203	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2110424	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2192413	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2192414	1.00[AMR][1000 genomes]
rs2192415	1.00[AMR][1000 genomes]
rs2192421	1.00[AMR][1000 genomes]
rs2215830	1.00[AMR][1000 genomes]
rs2215831	1.00[AMR][1000 genomes]
rs2215832	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2215833	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2366099	1.00[AMR][1000 genomes]
rs2366156	1.00[AMR][1000 genomes]
rs2886581	1.00[AMR][1000 genomes]
rs4899709	1.00[AMR][1000 genomes]
rs4899710	1.00[AMR][1000 genomes]
rs4903756	1.00[AMR][1000 genomes]
rs4903765	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6574444	1.00[AMR][1000 genomes]
rs6574449	1.00[AMR][1000 genomes]
rs7157498	1.00[AMR][1000 genomes]
rs7158579	1.00[AMR][1000 genomes]
rs7159492	1.00[AMR][1000 genomes]
rs8003367	1.00[AMR][1000 genomes]
rs8003391	1.00[AMR][1000 genomes]
rs8005882	1.00[AMR][1000 genomes]
rs8008949	1.00[AMR][1000 genomes]
rs8017182	1.00[AMR][1000 genomes]
rs8020682	1.00[AMR][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	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78946200-78951600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr14:78949600-78951800	Enhancers	Brain Germinal Matrix	brain
3	chr14:78950200-78955400	Weak transcription	Brain Angular Gyrus	brain
4	chr14:78950600-78951600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:78950600-78953000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:78950600-78953200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:78950800-78951200	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr14:78950800-78951800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr14:78950800-78953200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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