Variant report

Variant	rs2148066
Chromosome Location	chr13:95634181-95634182
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11616452	0.82[EUR][1000 genomes]
rs11617950	1.00[ASN][1000 genomes]
rs12856105	0.82[EUR][1000 genomes]
rs16950404	1.00[ASN][1000 genomes]
rs16950443	1.00[ASN][1000 genomes]
rs1925870	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1925876	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1925878	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1925879	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1952108	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2148064	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2148065	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2148067	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2182265	1.00[ASN][1000 genomes]
rs2209539	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2209540	1.00[ASN][1000 genomes]
rs2225007	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35781706	0.82[EUR][1000 genomes]
rs36113741	0.82[EUR][1000 genomes]
rs41386448	1.00[ASN][1000 genomes]
rs4238311	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4771903	0.84[ASN][1000 genomes]
rs55896076	1.00[ASN][1000 genomes]
rs55943137	1.00[ASN][1000 genomes]
rs60329452	1.00[ASN][1000 genomes]
rs60833033	0.91[ASN][1000 genomes]
rs61695658	1.00[ASN][1000 genomes]
rs6492758	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66562849	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66796852	0.91[ASN][1000 genomes]
rs67670273	0.91[ASN][1000 genomes]
rs71431487	0.82[EUR][1000 genomes]
rs72640796	1.00[ASN][1000 genomes]
rs72640799	1.00[ASN][1000 genomes]
rs72642310	1.00[ASN][1000 genomes]
rs72642313	1.00[ASN][1000 genomes]
rs72642322	0.91[ASN][1000 genomes]
rs72642324	0.91[ASN][1000 genomes]
rs7332543	0.91[ASN][1000 genomes]
rs7987195	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7988246	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7990475	1.00[ASN][1000 genomes]
rs8002563	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9302029	0.90[AFR][1000 genomes]
rs9302030	0.85[AFR][1000 genomes]
rs9302031	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9516503	0.82[EUR][1000 genomes]
rs9524709	1.00[CEU][hapmap]
rs9524731	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9524740	1.00[ASN][1000 genomes]
rs9524743	1.00[ASN][1000 genomes]
rs9524744	1.00[ASN][1000 genomes]
rs9524746	1.00[ASN][1000 genomes]
rs9584270	1.00[ASN][1000 genomes]
rs9590146	1.00[ASN][1000 genomes]
rs9590147	1.00[ASN][1000 genomes]
rs9590149	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9590153	1.00[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	nsv832688	chr13:95633193-95780198	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95627200-95635800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr13:95631400-95635800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:95633600-95635600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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