Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:106075494..106077166-chr8:106081357..106083896,2	MCF-7	breast:
2	chr8:106082822..106084651-chr8:106097372..106099591,2	K562	blood:
3	chr8:106082783..106085372-chr8:106087525..106090132,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1521777	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030476	1.00[ASN][1000 genomes]
rs2342483	1.00[ASN][1000 genomes]
rs28424250	1.00[ASN][1000 genomes]
rs285778	1.00[ASN][1000 genomes]
rs285797	0.81[EUR][1000 genomes]
rs285800	1.00[ASN][1000 genomes]
rs285808	1.00[ASN][1000 genomes]
rs285817	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285818	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285821	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285830	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285831	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285832	0.85[EUR][1000 genomes]
rs285844	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs285875	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28700873	1.00[ASN][1000 genomes]
rs364605	1.00[ASN][1000 genomes]
rs367858	1.00[ASN][1000 genomes]
rs398324	1.00[ASN][1000 genomes]
rs72676195	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762763	chr8:105943295-106218634	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv891253	chr8:105994885-106251476	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv891254	chr8:106060970-106175867	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	3 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	chr8:106081200-106083200	Enhancers	NH-A	brain
2	chr8:106081600-106083000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:106081600-106083000	Enhancers	NHDF-Ad	bronchial
4	chr8:106081800-106083200	Enhancers	Hela-S3	cervix
5	chr8:106081800-106083200	Enhancers	HUVEC	blood vessel
6	chr8:106081800-106083400	Enhancers	HSMM	muscle
7	chr8:106081800-106084000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:106082200-106084000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:106082200-106086200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:106082400-106085600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:106082600-106087600	Weak transcription	Fetal Heart	heart

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