Variant report

Variant	rs35898699
Chromosome Location	chr4:142438315-142438316
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10519602	0.89[EUR][1000 genomes]
rs12501765	0.87[EUR][1000 genomes]
rs12506151	0.88[EUR][1000 genomes]
rs12507564	0.88[EUR][1000 genomes]
rs12507887	0.88[EUR][1000 genomes]
rs12508511	0.89[EUR][1000 genomes]
rs12508590	0.89[EUR][1000 genomes]
rs12509285	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12509822	0.87[EUR][1000 genomes]
rs12510810	0.89[EUR][1000 genomes]
rs12511786	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12511918	0.89[EUR][1000 genomes]
rs12511983	0.89[EUR][1000 genomes]
rs13105639	0.88[EUR][1000 genomes]
rs13113365	0.92[EUR][1000 genomes]
rs13117984	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs13119177	0.91[EUR][1000 genomes]
rs13129076	0.88[EUR][1000 genomes]
rs13130612	0.88[EUR][1000 genomes]
rs13131082	0.88[EUR][1000 genomes]
rs13133795	0.88[EUR][1000 genomes]
rs13147873	0.90[EUR][1000 genomes]
rs1357158	0.92[EUR][1000 genomes]
rs1402811	0.92[EUR][1000 genomes]
rs1402812	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1436510	0.86[EUR][1000 genomes]
rs1521760	0.86[EUR][1000 genomes]
rs1521765	0.92[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs1521766	0.92[EUR][1000 genomes]
rs1554477	0.88[EUR][1000 genomes]
rs1581387	0.91[EUR][1000 genomes]
rs1581388	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1581390	0.92[EUR][1000 genomes]
rs1608019	0.91[EUR][1000 genomes]
rs17007301	0.88[EUR][1000 genomes]
rs17354547	0.88[EUR][1000 genomes]
rs17354568	0.88[EUR][1000 genomes]
rs1949667	0.87[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs2090878	0.88[EUR][1000 genomes]
rs2103007	0.88[EUR][1000 genomes]
rs2103008	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2322181	0.88[EUR][1000 genomes]
rs2322182	0.84[ASN][1000 genomes]
rs34132448	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs34147541	0.92[EUR][1000 genomes]
rs34585213	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34761999	0.91[EUR][1000 genomes]
rs34963107	0.89[EUR][1000 genomes]
rs35114853	0.92[EUR][1000 genomes]
rs35251884	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs35486128	0.91[EUR][1000 genomes]
rs35815487	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs35881750	0.92[EUR][1000 genomes]
rs36043837	0.89[EUR][1000 genomes]
rs4530710	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4956295	0.88[EUR][1000 genomes]
rs4956297	0.90[EUR][1000 genomes]
rs4956380	0.88[EUR][1000 genomes]
rs4956384	0.88[EUR][1000 genomes]
rs4956389	0.89[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs4956396	0.92[EUR][1000 genomes]
rs4956399	0.86[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs55726691	0.88[EUR][1000 genomes]
rs55912825	0.89[EUR][1000 genomes]
rs56029027	0.89[EUR][1000 genomes]
rs56051122	0.89[EUR][1000 genomes]
rs56074428	0.87[EUR][1000 genomes]
rs56140725	0.87[EUR][1000 genomes]
rs56155233	0.89[EUR][1000 genomes]
rs60008610	0.87[EUR][1000 genomes]
rs62326572	0.90[EUR][1000 genomes]
rs62326579	0.90[EUR][1000 genomes]
rs62326617	0.89[EUR][1000 genomes]
rs68056864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6810477	0.87[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs6812950	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs6816897	0.89[EUR][1000 genomes]
rs6818965	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6825913	0.88[EUR][1000 genomes]
rs6826356	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs6829748	0.87[EUR][1000 genomes]
rs6831141	0.88[EUR][1000 genomes]
rs6838410	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6842807	0.89[EUR][1000 genomes]
rs6845550	0.88[EUR][1000 genomes]
rs6852094	0.84[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6858423	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7666040	0.86[ASN][1000 genomes]
rs7666229	0.86[ASN][1000 genomes]
rs7671408	0.88[EUR][1000 genomes]
rs7677830	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9761396	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880172	chr4:142355535-142565089	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830094	chr4:142411738-142567788	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:142435400-142443200	Weak transcription	Aorta	Aorta

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