Variant report

Variant	rs34101282
Chromosome Location	chr1:186617478-186617479
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10489397	0.81[EUR][1000 genomes]
rs10911899	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11799322	0.81[EUR][1000 genomes]
rs11802553	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11804161	0.81[EUR][1000 genomes]
rs11806329	0.81[EUR][1000 genomes]
rs11806663	0.81[EUR][1000 genomes]
rs11807318	0.81[EUR][1000 genomes]
rs11807443	0.81[EUR][1000 genomes]
rs11808900	0.81[EUR][1000 genomes]
rs11810534	0.81[EUR][1000 genomes]
rs11811047	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12239058	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12726528	0.81[EUR][1000 genomes]
rs12726764	0.81[EUR][1000 genomes]
rs12731687	0.81[EUR][1000 genomes]
rs12732584	0.84[AMR][1000 genomes]
rs12734267	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12734420	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12739643	0.81[EUR][1000 genomes]
rs12747991	0.81[EUR][1000 genomes]
rs12753223	0.81[EUR][1000 genomes]
rs16825639	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16825646	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16825671	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16825681	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16825687	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1883650	0.81[EUR][1000 genomes]
rs1883651	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1883652	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2891249	0.81[EUR][1000 genomes]
rs2891250	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34200789	0.81[EUR][1000 genomes]
rs34365031	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34770837	0.86[EUR][1000 genomes]
rs35084661	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35205448	0.81[EUR][1000 genomes]
rs35240980	0.81[EUR][1000 genomes]
rs35461575	0.81[EUR][1000 genomes]
rs35483551	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36016361	0.81[EUR][1000 genomes]
rs36030781	0.81[EUR][1000 genomes]
rs4511065	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6683271	0.81[EUR][1000 genomes]
rs71634178	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs71634179	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71634186	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv832059	chr1:186464932-186639125	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762854	chr1:186547101-186847574	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186613200-186617600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:186613600-186619400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:186614400-186619600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:186616400-186618400	Enhancers	Ovary	ovary

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