Variant report

Variant	rs1987136
Chromosome Location	chr9:108683022-108683023
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10114385	0.81[EUR][1000 genomes]
rs10115085	0.87[CEU][hapmap];0.85[MEX][hapmap];0.81[EUR][1000 genomes]
rs10117602	0.87[CEU][hapmap];0.85[MEX][hapmap];0.81[EUR][1000 genomes]
rs10120538	0.87[CEU][hapmap];0.85[MEX][hapmap]
rs10123374	0.81[EUR][1000 genomes]
rs10759149	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10759150	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10759151	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10759152	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10759153	0.81[EUR][1000 genomes]
rs10816353	0.93[ASN][1000 genomes]
rs10978330	0.82[EUR][1000 genomes]
rs10978340	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10978359	0.84[ASN][1000 genomes]
rs16925032	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs1961970	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1987247	0.99[ASN][1000 genomes]
rs2417644	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2417658	0.97[ASN][1000 genomes]
rs2417659	0.93[ASN][1000 genomes]
rs2417660	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900404	0.81[EUR][1000 genomes]
rs3884524	0.94[ASN][1000 genomes]
rs4598317	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4742967	0.81[EUR][1000 genomes]
rs4742969	0.83[EUR][1000 genomes]
rs4742974	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4742975	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6477482	0.81[EUR][1000 genomes]
rs7025973	0.87[CEU][hapmap];0.85[MEX][hapmap];0.81[EUR][1000 genomes]
rs7030289	0.90[ASN][1000 genomes]
rs7040788	0.87[CEU][hapmap];0.84[MEX][hapmap];0.81[EUR][1000 genomes]
rs7040794	0.81[EUR][1000 genomes]
rs7043384	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7044156	0.81[EUR][1000 genomes]
rs72732742	0.94[ASN][1000 genomes]
rs7851747	0.97[ASN][1000 genomes]
rs7856876	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv893694	chr9:108486533-108854018	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1041073	chr9:108535813-108731343	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1052684	chr9:108582944-108730280	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv615140	chr9:108592589-108725567	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv831679	chr9:108603112-108785347	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108674000-108683600	Weak transcription	Left Ventricle	heart
2	chr9:108674600-108683600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:108681400-108683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr9:108682800-108684200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:108683000-108683400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:108683000-108683800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr9:108683000-108684600	Enhancers	Fetal Heart	heart

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