Variant report

Variant	rs9839573
Chromosome Location	chr3:134612190-134612191
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10935140	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11706968	0.85[JPT][hapmap]
rs12489360	0.88[JPT][hapmap]
rs12630436	0.83[JPT][hapmap]
rs13068347	0.81[JPT][hapmap]
rs13073341	0.83[JPT][hapmap]
rs13078906	0.88[JPT][hapmap]
rs1399706	0.88[JPT][hapmap]
rs1399707	0.81[JPT][hapmap]
rs1515359	0.96[CEU][hapmap];0.92[CHB][hapmap];0.87[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1515364	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1515366	0.88[JPT][hapmap]
rs2280157	0.83[JPT][hapmap]
rs2895696	0.94[JPT][hapmap]
rs4955458	0.93[JPT][hapmap];0.80[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4955508	0.94[JPT][hapmap]
rs4955510	0.87[JPT][hapmap]
rs4955511	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6439530	0.81[JPT][hapmap]
rs6439535	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6762621	0.81[JPT][hapmap];0.80[YRI][hapmap];0.86[AFR][1000 genomes]
rs6779978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6786490	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6789449	0.81[JPT][hapmap]
rs6793377	0.88[JPT][hapmap]
rs6796514	0.81[JPT][hapmap]
rs6802089	0.81[JPT][hapmap]
rs7639520	0.93[JPT][hapmap]
rs7639843	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7643782	0.88[JPT][hapmap]
rs7645886	0.88[JPT][hapmap]
rs7653227	0.81[JPT][hapmap]
rs868130	0.94[JPT][hapmap]
rs884381	0.94[JPT][hapmap]
rs938382	0.94[JPT][hapmap]
rs9814692	0.87[JPT][hapmap]
rs9819889	0.94[JPT][hapmap]
rs9825632	0.83[JPT][hapmap]
rs9825687	0.88[JPT][hapmap]
rs9846488	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9851596	0.94[JPT][hapmap]
rs9868348	0.87[JPT][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9874291	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9874607	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009634	chr3:134543259-134820208	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv536720	chr3:134543259-134820208	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1000277	chr3:134546080-134970837	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134599800-134613400	Weak transcription	Fetal Brain Female	brain
2	chr3:134610800-134612200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr3:134610800-134612400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr3:134610800-134617400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr3:134611000-134612600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr3:134611000-134612600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr3:134611000-134612800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:134611000-134613400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:134611200-134612200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr3:134611200-134612200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr3:134611200-134616200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:134611400-134619600	Weak transcription	GM12878-XiMat	blood
13	chr3:134611800-134612200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr3:134612000-134612200	Enhancers	Brain Germinal Matrix	brain

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