Variant report

Variant	rs4133033
Chromosome Location	chr9:95675013-95675014
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:95668983..95671268-chr9:95672944..95675033,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10115872	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10123843	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10123870	0.88[EUR][1000 genomes]
rs10156497	0.82[ASN][1000 genomes]
rs1022833	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10739932	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10739933	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10739934	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10761172	0.82[ASN][1000 genomes]
rs10761175	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10821021	0.82[ASN][1000 genomes]
rs10821022	0.82[ASN][1000 genomes]
rs10821028	0.82[ASN][1000 genomes]
rs10821030	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821031	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821032	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10821035	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821040	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992489	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10992529	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12336022	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12337654	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12338961	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12346689	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12379300	0.82[ASN][1000 genomes]
rs13288901	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13294147	0.83[ASN][1000 genomes]
rs35449185	0.83[ASN][1000 genomes]
rs36194652	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3824428	0.82[ASN][1000 genomes]
rs4510923	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4535796	0.97[ASN][1000 genomes]
rs4538949	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4626670	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744150	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4744151	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6479434	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7024752	0.83[ASN][1000 genomes]
rs7032277	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7035868	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7039812	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7040645	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7045305	0.82[ASN][1000 genomes]
rs7047181	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7847713	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7847998	0.82[ASN][1000 genomes]
rs7869480	0.82[ASN][1000 genomes]
rs7872848	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7872987	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7873021	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7874026	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][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	nsv831654	chr9:95542920-95720961	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv893574	chr9:95580376-95688099	Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv1818795	chr9:95656340-95689158	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
4	nsv982639	chr9:95671744-95685131	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95673800-95675200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:95674000-95675200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:95674400-95675200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr9:95674400-95675400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:95674400-95675400	Bivalent Enhancer	Fetal Brain Male	brain
6	chr9:95674400-95675600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:95674400-95675800	Enhancers	Lung	lung
8	chr9:95674400-95679800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr9:95674600-95675200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
10	chr9:95674600-95675400	Bivalent Enhancer	A549	lung
11	chr9:95674600-95679400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr9:95674800-95675800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:95674800-95687400	Weak transcription	Right Atrium	heart
14	chr9:95675000-95675200	Enhancers	Brain Germinal Matrix	brain
15	chr9:95675000-95675400	Bivalent Enhancer	Fetal Stomach	stomach

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