Variant report

Variant	rs4943444
Chromosome Location	chr13:37724153-37724154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1009963	0.82[EUR][1000 genomes]
rs11147628	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11147629	0.87[EUR][1000 genomes]
rs11147630	0.87[EUR][1000 genomes]
rs11147632	0.87[EUR][1000 genomes]
rs11620134	0.87[EUR][1000 genomes]
rs1199995	0.83[EUR][1000 genomes]
rs1199996	0.83[EUR][1000 genomes]
rs12583685	0.87[EUR][1000 genomes]
rs12584417	0.87[EUR][1000 genomes]
rs12585998	0.87[EUR][1000 genomes]
rs1336754	0.86[EUR][1000 genomes]
rs1336762	0.87[EUR][1000 genomes]
rs1764480	0.83[EUR][1000 genomes]
rs1781669	0.83[EUR][1000 genomes]
rs1781670	0.83[EUR][1000 genomes]
rs1856028	0.86[EUR][1000 genomes]
rs1856029	0.85[EUR][1000 genomes]
rs1937756	0.81[EUR][1000 genomes]
rs1937757	0.84[EUR][1000 genomes]
rs1937758	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2997194	0.81[EUR][1000 genomes]
rs3904094	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57671308	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs58229785	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6563511	0.88[EUR][1000 genomes]
rs7327617	0.87[EUR][1000 genomes]
rs7334447	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7335490	0.86[EUR][1000 genomes]
rs7981360	0.88[EUR][1000 genomes]
rs7996099	0.83[EUR][1000 genomes]
rs7996605	0.88[EUR][1000 genomes]
rs7996662	0.88[EUR][1000 genomes]
rs8003010	0.83[EUR][1000 genomes]
rs945632	0.86[EUR][1000 genomes]
rs9566176	0.82[EUR][1000 genomes]
rs9566181	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9566182	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9566183	0.87[EUR][1000 genomes]
rs9566184	0.88[EUR][1000 genomes]
rs9566185	0.88[EUR][1000 genomes]
rs9566186	0.88[EUR][1000 genomes]
rs9566187	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576171	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9576172	0.83[EUR][1000 genomes]
rs9576173	0.83[EUR][1000 genomes]
rs9576184	0.86[EUR][1000 genomes]
rs9576185	0.86[EUR][1000 genomes]
rs9576186	0.88[EUR][1000 genomes]
rs9576187	0.88[EUR][1000 genomes]
rs9576188	0.88[EUR][1000 genomes]
rs9576189	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9576190	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9576192	0.87[AMR][1000 genomes];0.84[EUR][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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37722400-37740600	Weak transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links