Variant report

Variant	rs11142926
Chromosome Location	chr9:71176227-71176228
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:71175109..71177621-chr9:71180020..71182524,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11142941	0.95[CHB][hapmap];0.91[JPT][hapmap];0.95[ASN][1000 genomes]
rs1571825	0.88[ASN][1000 genomes]
rs1571826	0.88[ASN][1000 genomes]
rs4745107	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7029779	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893413	chr9:71130848-71196984	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893411	chr9:71130848-71199545	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv893412	chr9:71130848-71199545	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1024967	chr9:71130848-71210031	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv482506	chr9:71130848-71280888	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv466392	chr9:71130848-71318817	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv614546	chr9:71130848-71318817	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv893414	chr9:71139378-71320732	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71173200-71177600	Enhancers	Primary hematopoietic stem cells	blood
2	chr9:71174200-71181600	Weak transcription	Gastric	stomach
3	chr9:71174600-71176400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:71175200-71181000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr9:71175400-71177400	Enhancers	Primary B cells from cord blood	blood
6	chr9:71175400-71179600	Weak transcription	Pancreas	Pancrea
7	chr9:71175600-71176400	Enhancers	NHLF	lung
8	chr9:71175800-71176400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr9:71175800-71176600	Weak transcription	Fetal Intestine Large	intestine
10	chr9:71175800-71177000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:71175800-71177400	Weak transcription	Lung	lung
12	chr9:71175800-71178400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:71175800-71179600	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:71175800-71179600	Weak transcription	Left Ventricle	heart
15	chr9:71175800-71179800	Weak transcription	Stomach Mucosa	stomach
16	chr9:71175800-71183400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr9:71176000-71177200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr9:71176200-71177200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:71176200-71177200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr9:71176200-71177400	Weak transcription	Fetal Kidney	kidney
21	chr9:71176200-71178200	Weak transcription	Fetal Stomach	stomach
22	chr9:71176200-71178800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:71176200-71180000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:71176200-71180800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:71176200-71182200	Weak transcription	Colon Smooth Muscle	Colon
26	chr9:71176200-71182200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr9:71176200-71182400	Weak transcription	Rectal Smooth Muscle	rectum

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