Variant report

Variant	rs34335232
Chromosome Location	chr1:170265691-170265692
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10753803	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10800510	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10800511	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11577543	0.95[ASN][1000 genomes]
rs11579802	0.84[ASN][1000 genomes]
rs11582930	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11585499	0.84[ASN][1000 genomes]
rs11802454	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11802884	0.93[ASN][1000 genomes]
rs12404913	0.91[ASN][1000 genomes]
rs12725915	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12738543	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12745998	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1332955	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2095134	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2151244	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2151245	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2184041	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2184042	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2251095	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2254605	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2254608	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2254609	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2265323	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2990635	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2990637	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2990638	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2990639	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2990641	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2998163	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2998165	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2998166	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35038938	0.87[ASN][1000 genomes]
rs35102909	0.89[ASN][1000 genomes]
rs3795614	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3795615	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55834059	0.96[ASN][1000 genomes]
rs56185457	0.95[ASN][1000 genomes]
rs61827994	0.85[ASN][1000 genomes]
rs61827996	0.85[ASN][1000 genomes]
rs6700678	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7522187	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7524746	0.91[ASN][1000 genomes]
rs7538465	0.86[ASN][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	nsv1014033	chr1:169968488-170453021	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv535200	chr1:169968488-170453021	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170254600-170267800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:170261400-170265800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:170265200-170266000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:170265400-170266200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:170265400-170266200	Enhancers	NHDF-Ad	bronchial

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