Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11527400..11529595-chr8:11534511..11536645,2	K562	blood:

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

rs_ID	r²[population]
rs2264310	1.00[AMR][1000 genomes]
rs58313162	1.00[AMR][1000 genomes]
rs7010515	1.00[AMR][1000 genomes]
rs7014537	1.00[AMR][1000 genomes]
rs73531781	1.00[AMR][1000 genomes]
rs73535989	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73535990	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73535993	1.00[AMR][1000 genomes]
rs73537868	1.00[AMR][1000 genomes]
rs73545763	1.00[AMR][1000 genomes]
rs73545769	1.00[AMR][1000 genomes]
rs7818491	1.00[AMR][1000 genomes]
rs7824489	1.00[AMR][1000 genomes]
rs7837707	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8191524	1.00[AMR][1000 genomes]
rs8191532	1.00[AMR][1000 genomes]
rs8191533	1.00[AMR][1000 genomes]
rs8191580	1.00[AMR][1000 genomes]
rs8191628	1.00[AMR][1000 genomes]
rs8191653	1.00[AMR][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	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11527800-11529000	Enhancers	Stomach Mucosa	stomach
2	chr8:11527800-11529600	Enhancers	Fetal Intestine Small	intestine
3	chr8:11528000-11529000	Enhancers	Duodenum Mucosa	Duodenum
4	chr8:11528000-11529800	Enhancers	Ovary	ovary
5	chr8:11528600-11529000	Bivalent Enhancer	Fetal Intestine Large	intestine
6	chr8:11528600-11529400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr8:11528600-11529600	Enhancers	Liver	Liver
8	chr8:11528600-11529800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr8:11528800-11529200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr8:11528800-11529400	Bivalent Enhancer	HSMM	muscle
11	chr8:11528800-11534400	Weak transcription	Gastric	stomach
12	chr8:11528800-11547200	Weak transcription	Pancreas	Pancrea

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