Variant report

Variant	rs35593664
Chromosome Location	chr3:68809881-68809882
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11128090	1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12054044	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12629295	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12632377	0.96[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12633144	1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12635072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12638859	1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13062535	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13066315	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13093729	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13095333	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13097433	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17047942	0.86[AMR][1000 genomes]
rs17047968	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17047978	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17047979	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17047991	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1948291	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1994592	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1994593	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs34006637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs34098780	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs34285930	0.93[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs34668623	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34720222	0.83[AMR][1000 genomes]
rs34903671	0.86[AMR][1000 genomes]
rs34919495	0.93[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs35132255	0.84[AMR][1000 genomes]
rs35270691	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35336306	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs35586328	0.89[AMR][1000 genomes]
rs35740552	0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35768765	1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs35868242	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35912963	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4855342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4855509	1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4855510	0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4855511	0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4855520	0.86[AMR][1000 genomes]
rs4855525	0.86[AMR][1000 genomes]
rs4855526	0.86[AMR][1000 genomes]
rs56909663	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60226140	0.86[AMR][1000 genomes]
rs6763155	0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6774520	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6774607	1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6801847	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs71302144	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs71302145	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71302146	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71302148	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7642323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs8180031	0.84[AMR][1000 genomes]
rs902246	0.88[ASN][1000 genomes]
rs902247	0.88[ASN][1000 genomes]
rs9815927	0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr3:68807800-68811000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:68808000-68810800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:68808200-68811200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:68808400-68810200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:68808400-68813200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:68808800-68810200	Enhancers	Fetal Brain Male	brain
7	chr3:68808800-68813200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:68809000-68811000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:68809200-68813200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr3:68809200-68813600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:68809600-68811000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:68809800-68810200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:68809800-68810200	Enhancers	H9 Cell Line	embryonic stem cell

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