Variant report

Variant	rs8031192
Chromosome Location	chr15:55989080-55989081
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1014551	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs11857453	0.96[ASN][1000 genomes]
rs11857467	0.97[ASN][1000 genomes]
rs11858195	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12594642	0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1371056	0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1530087	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1550330	0.92[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.85[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16976466	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs1814329	0.84[CEU][hapmap]
rs1986012	0.84[ASN][1000 genomes]
rs2414424	0.82[AMR][1000 genomes]
rs2414426	0.86[AMR][1000 genomes]
rs2414427	0.82[AMR][1000 genomes]
rs4774802	0.81[JPT][hapmap]
rs59820715	0.92[ASN][1000 genomes]
rs62043872	0.81[AMR][1000 genomes]
rs6493805	0.81[AMR][1000 genomes]
rs687128	0.88[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs71110312	0.81[AMR][1000 genomes]
rs715321	0.86[AMR][1000 genomes]
rs7162071	0.89[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs7359255	0.84[CEU][hapmap]
rs8043521	0.88[ASN][1000 genomes]
rs9672390	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv948522	chr15:55639867-56032099	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv1049774	chr15:55759573-56044600	Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55960800-55995800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:55986600-55989200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:55986800-55992600	Weak transcription	GM12878-XiMat	blood
4	chr15:55987200-55989800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:55987600-55995600	Weak transcription	Fetal Kidney	kidney
6	chr15:55987800-55996000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:55988000-55997200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:55988200-55993800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:55988400-55989600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr15:55988400-55995000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:55988400-55995600	Weak transcription	Hela-S3	cervix
12	chr15:55988800-55989200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:55988800-55991400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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