Variant report

Variant	rs9431436
Chromosome Location	chr1:221361722-221361723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10218738	0.81[EUR][1000 genomes]
rs10218739	0.81[EUR][1000 genomes]
rs10489957	0.95[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1073166	0.83[EUR][1000 genomes]
rs10746408	0.83[EUR][1000 genomes]
rs10779421	0.81[EUR][1000 genomes]
rs10863584	0.80[EUR][1000 genomes]
rs10863585	0.83[EUR][1000 genomes]
rs10863589	0.92[EUR][1000 genomes]
rs11118650	0.81[EUR][1000 genomes]
rs11118657	0.95[EUR][1000 genomes]
rs12408324	0.95[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1372665	0.83[EUR][1000 genomes]
rs1417921	0.85[EUR][1000 genomes]
rs1442465	0.81[EUR][1000 genomes]
rs1539139	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17009643	0.84[AFR][1000 genomes]
rs1867071	0.81[EUR][1000 genomes]
rs1965817	0.83[EUR][1000 genomes]
rs1992480	0.81[EUR][1000 genomes]
rs2378435	0.81[EUR][1000 genomes]
rs4518910	0.81[EUR][1000 genomes]
rs4532839	0.84[EUR][1000 genomes]
rs4846689	0.88[ASN][1000 genomes]
rs6541171	0.81[EUR][1000 genomes]
rs6541172	0.81[EUR][1000 genomes]
rs6541179	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6541180	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6656408	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6656596	0.81[EUR][1000 genomes]
rs6657690	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6664595	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669742	0.81[EUR][1000 genomes]
rs6677416	0.81[EUR][1000 genomes]
rs6696268	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7513152	0.81[EUR][1000 genomes]
rs7527151	0.81[EUR][1000 genomes]
rs7527891	0.81[EUR][1000 genomes]
rs7545437	0.81[EUR][1000 genomes]
rs894361	0.81[EUR][1000 genomes]
rs9431421	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9431432	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs989463	0.83[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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873199	chr1:221136672-221451217	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221360400-221362200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:221360800-221362200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr1:221361400-221362400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr1:221361600-221362200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links