Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:25654125..25655880-chr6:25659519..25661967,2	K562	blood:

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10456325	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12195457	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12201249	0.86[ASN][1000 genomes]
rs1883257	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1884575	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6913169	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6918563	0.86[ASN][1000 genomes]
rs72840515	0.93[ASN][1000 genomes]
rs72840523	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72840524	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72840525	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7741026	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9461190	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9467544	0.93[ASN][1000 genomes]
rs9467555	0.86[AMR][1000 genomes];1.00[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	nsv883488	chr6:25592489-25731691	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
4	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25658600-25665000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr6:25659800-25661000	Enhancers	HepG2	liver
3	chr6:25660000-25661400	Enhancers	HSMM	muscle
4	chr6:25660000-25662000	Enhancers	Fetal Intestine Small	intestine
5	chr6:25660200-25661000	Enhancers	HSMMtube	muscle
6	chr6:25660200-25661200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:25660200-25661600	Enhancers	HMEC	breast
8	chr6:25660200-25662000	Enhancers	Liver	Liver
9	chr6:25660200-25662000	Enhancers	Fetal Intestine Large	intestine
10	chr6:25660400-25661000	Enhancers	Pancreas	Pancrea
11	chr6:25660400-25661400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:25660400-25661800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:25660400-25661800	Enhancers	NHEK	skin
14	chr6:25660600-25661000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:25660600-25661000	Flanking Active TSS	A549	lung
16	chr6:25660600-25661200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr6:25660600-25661200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr6:25660600-25661200	Enhancers	Hela-S3	cervix
19	chr6:25660600-25661200	Enhancers	HUVEC	blood vessel
20	chr6:25660600-25671400	Weak transcription	Stomach Mucosa	stomach
21	chr6:25660800-25661200	Enhancers	NHDF-Ad	bronchial

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