Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:107590391..107592343-chr8:107594481..107597420,2	K562	blood:

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

rs_ID	r²[population]
rs1462810	0.84[ASN][1000 genomes]
rs2045786	0.81[ASN][1000 genomes]
rs3101526	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs3101542	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs3101543	0.88[CHB][hapmap];0.81[ASN][1000 genomes]
rs3101545	0.84[ASN][1000 genomes]
rs3101546	0.84[ASN][1000 genomes]
rs3101548	0.82[CHB][hapmap]
rs3110421	0.83[CHB][hapmap]
rs3110423	0.83[CHB][hapmap]
rs3110430	0.94[CHB][hapmap];0.97[ASN][1000 genomes]
rs3110433	0.84[ASN][1000 genomes]
rs3110434	0.81[ASN][1000 genomes]
rs3110435	0.81[ASN][1000 genomes]
rs3110775	0.84[ASN][1000 genomes]
rs3132803	0.82[CHB][hapmap]
rs3134121	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3134125	1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3134142	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs72680983	0.82[AMR][1000 genomes];0.82[ASN][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	nsv533134	chr8:107307812-107670002	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3417701	chr8:107595449-107595977	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107512400-107620200	Weak transcription	Aorta	Aorta
2	chr8:107590200-107601400	Weak transcription	Pancreas	Pancrea
3	chr8:107592400-107606600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:107594200-107601200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:107594800-107600600	Weak transcription	Fetal Intestine Large	intestine

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