Variant report

Variant	rs2897114
Chromosome Location	chr1:47522988-47522989
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1039468	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1039469	0.88[AMR][1000 genomes]
rs11211420	0.91[ASN][1000 genomes]
rs11211424	0.92[ASN][1000 genomes]
rs11211425	0.92[ASN][1000 genomes]
rs11211426	0.92[ASN][1000 genomes]
rs11211441	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11211445	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11582907	0.86[ASN][1000 genomes]
rs11584372	0.92[ASN][1000 genomes]
rs11584400	0.91[ASN][1000 genomes]
rs12030385	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12041262	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12041324	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12045381	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12140891	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12141009	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12402481	0.92[ASN][1000 genomes]
rs12406683	0.91[ASN][1000 genomes]
rs12408055	0.89[ASN][1000 genomes]
rs12408938	0.91[ASN][1000 genomes]
rs1502909	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1553390	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17102972	0.91[ASN][1000 genomes]
rs17102977	0.91[ASN][1000 genomes]
rs17102978	0.91[ASN][1000 genomes]
rs1827473	0.83[AMR][1000 genomes]
rs1847225	0.80[EUR][1000 genomes]
rs1963620	0.87[AMR][1000 genomes]
rs1986925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2036462	0.89[AMR][1000 genomes]
rs2202221	0.92[ASN][1000 genomes]
rs2202222	0.92[ASN][1000 genomes]
rs2221324	0.91[ASN][1000 genomes]
rs2292059	0.89[ASN][1000 genomes]
rs2292060	0.91[ASN][1000 genomes]
rs35322032	0.80[ASN][1000 genomes]
rs3920100	0.91[ASN][1000 genomes]
rs4926728	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4926776	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55694114	0.90[ASN][1000 genomes]
rs55909645	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59244133	0.83[ASN][1000 genomes]
rs66753730	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6682257	0.81[EUR][1000 genomes]
rs72637973	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs74073884	0.91[ASN][1000 genomes]
rs74073885	0.91[ASN][1000 genomes]
rs7549836	0.83[ASN][1000 genomes]
rs9699826	0.92[ASN][1000 genomes]
rs9699991	0.92[ASN][1000 genomes]
rs9700422	0.91[ASN][1000 genomes]
rs9701888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9793989	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009338	chr1:47358532-47555253	Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2763300	chr1:47358532-47628774	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv916813	chr1:47435635-47666179	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv871717	chr1:47449486-47524264	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv461428	chr1:47487585-47524264	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv546167	chr1:47487585-47524264	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 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	chr1:47515400-47524000	Weak transcription	Aorta	Aorta
2	chr1:47516000-47523600	Weak transcription	Left Ventricle	heart

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