Variant report

Variant	rs1147785
Chromosome Location	chr9:13364330-13364331
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1147780	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1147781	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1169101	0.87[AMR][1000 genomes]
rs1169237	1.00[EUR][1000 genomes]
rs1185646	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1330141	0.87[AMR][1000 genomes]
rs1330144	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1813890	0.87[AMR][1000 genomes]
rs2183353	0.87[AMR][1000 genomes]
rs903320	0.87[AMR][1000 genomes];0.87[EUR][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	nsv892578	chr9:12942956-13485035	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv427838	chr9:13229753-13393890	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2752281	chr9:13284600-13405072	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv831515	chr9:13333205-13517308	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr9:13358600-13365600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:13358600-13369000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:13358800-13369000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:13360400-13369000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:13361800-13364400	Weak transcription	Colon Smooth Muscle	Colon
6	chr9:13362000-13364400	Weak transcription	Adipose Nuclei	Adipose
7	chr9:13362000-13365200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:13362200-13369000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:13364000-13364400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:13364000-13365200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:13364200-13365000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:13364200-13365000	Enhancers	Cortex derived primary cultured neurospheres	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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