Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:156106149..156107857-chr3:156114527..156116715,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12054064	1.00[CEU][hapmap]
rs13315734	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1357434	1.00[CEU][hapmap]
rs16826030	1.00[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs16826100	1.00[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs16826101	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs16826111	0.91[EUR][1000 genomes]
rs17238588	0.91[EUR][1000 genomes]
rs17317344	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2272112	1.00[CEU][hapmap]
rs3755633	1.00[CEU][hapmap]
rs3856672	0.91[EUR][1000 genomes]
rs58590195	1.00[ASN][1000 genomes]
rs6441062	0.82[EUR][1000 genomes]
rs6441068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6441072	1.00[CEU][hapmap]
rs6791462	1.00[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs73873328	1.00[EUR][1000 genomes]
rs73873329	1.00[EUR][1000 genomes]
rs7640596	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs9823622	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9824778	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs9844410	0.82[EUR][1000 genomes]
rs9847596	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9855009	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs9867561	1.00[EUR][1000 genomes]
rs9872444	1.00[EUR][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	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv1806015	chr3:156095513-156114898	Weak transcription Enhancers Bivalent Enhancer	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	chr3:156108200-156117000	Weak transcription	HSMMtube	muscle
2	chr3:156111200-156161600	Weak transcription	Aorta	Aorta
3	chr3:156113400-156115600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:156113600-156115400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:156113600-156115400	Enhancers	Colon Smooth Muscle	Colon
6	chr3:156113600-156115800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:156114000-156115400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:156114000-156115800	Enhancers	NHDF-Ad	bronchial
9	chr3:156114600-156115200	Weak transcription	Fetal Kidney	kidney
10	chr3:156114600-156115600	Enhancers	Rectal Smooth Muscle	rectum

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