Variant report

Variant	rs315381
Chromosome Location	chr4:73741350-73741351
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11730890	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11731791	0.96[ASN][1000 genomes]
rs11930953	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1426013	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1461524	0.87[ASN][1000 genomes]
rs1541754	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1593448	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1593451	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1813161	0.91[ASN][1000 genomes]
rs1813162	0.91[ASN][1000 genomes]
rs1813163	0.90[ASN][1000 genomes]
rs2010756	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2194933	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4694567	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60589574	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6446894	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6446895	0.91[ASN][1000 genomes]
rs6810425	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6822170	0.91[ASN][1000 genomes]
rs6825201	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6829946	0.86[ASN][1000 genomes]
rs6832369	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6833453	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7377303	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7440448	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7657580	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7665035	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7676987	0.90[ASN][1000 genomes]
rs7688481	0.87[ASN][1000 genomes]
rs7690017	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7698530	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7699324	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7700231	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949371	chr4:73678470-74094500	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv2757068	chr4:73683018-73770378	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2759261	chr4:73683018-73770378	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv436952	chr4:73693532-73759117	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv437923	chr4:73699066-73758650	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv818243	chr4:73707973-73758511	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1005704	chr4:73708248-73907315	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv829971	chr4:73709753-73880451	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1014364	chr4:73724140-73771587	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv432611	chr4:73740665-74099265	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 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	chr4:73740600-73741600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:73740800-73741600	Enhancers	Aorta	Aorta

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