Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:49374336..49376781-chr13:49377501..49380255,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10220140	0.88[ASN][1000 genomes]
rs12100214	0.82[ASN][1000 genomes]
rs12429439	0.87[ASN][1000 genomes]
rs1536136	0.87[ASN][1000 genomes]
rs1868550	0.85[ASN][1000 genomes]
rs2057585	0.85[ASN][1000 genomes]
rs2122278	0.85[ASN][1000 genomes]
rs58519664	0.82[ASN][1000 genomes]
rs6561479	0.85[ASN][1000 genomes]
rs732769	0.91[ASN][1000 genomes]
rs7330742	0.82[ASN][1000 genomes]
rs7337637	0.91[ASN][1000 genomes]
rs73480227	0.89[ASN][1000 genomes]
rs7989311	0.96[ASN][1000 genomes]
rs8000501	0.82[ASN][1000 genomes]
rs959353	0.85[CEU][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9595988	0.85[ASN][1000 genomes]
rs9595995	0.89[ASN][1000 genomes]
rs9595997	0.91[ASN][1000 genomes]
rs9596011	0.93[ASN][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	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv2758327	chr13:49283983-49472517	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2759936	chr13:49283983-49472517	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv832606	chr13:49352212-49506009	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49366800-49383000	Weak transcription	Osteobl	bone
2	chr13:49375800-49379000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr13:49376000-49379000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr13:49376000-49383400	Weak transcription	NHLF	lung
5	chr13:49376200-49379000	Weak transcription	NHDF-Ad	bronchial
6	chr13:49376200-49379200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr13:49376400-49378800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr13:49376400-49379000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr13:49378000-49380600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:49378200-49379600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr13:49378400-49380400	Enhancers	Primary T helper cells fromperipheralblood	blood

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