Variant report

Variant	rs9548637
Chromosome Location	chr13:39694176-39694177
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:56)

rs_ID	r²[population]
rs10162135	0.92[ASN][1000 genomes]
rs10467464	0.95[ASN][1000 genomes]
rs10870730	0.94[ASN][1000 genomes]
rs1333435	0.95[ASN][1000 genomes]
rs1333436	0.95[ASN][1000 genomes]
rs1333437	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1359653	0.81[AMR][1000 genomes]
rs1359654	0.81[AMR][1000 genomes]
rs1413042	0.94[ASN][1000 genomes]
rs1413043	0.94[ASN][1000 genomes]
rs1887108	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1887109	0.81[AMR][1000 genomes]
rs2324129	0.81[AMR][1000 genomes]
rs2324130	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4270047	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4941905	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4943631	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4943632	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4943639	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6563680	0.96[ASN][1000 genomes]
rs6563683	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs726051	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7321413	0.95[ASN][1000 genomes]
rs7328891	0.84[ASN][1000 genomes]
rs7334550	0.95[ASN][1000 genomes]
rs7336775	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7990331	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7990542	0.81[AMR][1000 genomes]
rs7997688	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7998548	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9315652	0.81[AMR][1000 genomes]
rs9315653	0.81[AMR][1000 genomes]
rs9315654	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9315655	0.95[ASN][1000 genomes]
rs9315656	0.96[ASN][1000 genomes]
rs9532332	0.95[ASN][1000 genomes]
rs9548614	0.81[AMR][1000 genomes]
rs9548615	0.81[AMR][1000 genomes]
rs9548616	0.81[AMR][1000 genomes]
rs9548618	0.81[AMR][1000 genomes]
rs9548619	0.81[AMR][1000 genomes]
rs9548620	0.81[AMR][1000 genomes]
rs9548639	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548640	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9548643	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9548644	0.87[ASN][1000 genomes]
rs9548645	0.80[ASN][1000 genomes]
rs9566403	0.80[ASN][1000 genomes]
rs9576732	0.95[ASN][1000 genomes]
rs9576733	0.95[ASN][1000 genomes]
rs9576735	0.94[ASN][1000 genomes]
rs9576738	0.96[ASN][1000 genomes]
rs9576739	0.92[ASN][1000 genomes]
rs9576740	0.92[ASN][1000 genomes]
rs9603510	1.00[ASN][1000 genomes]
rs9603512	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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
2	nsv1035255	chr13:39618302-39715336	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39693600-39699000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:39694000-39694400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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