Variant report

Variant	rs1231726
Chromosome Location	chr1:192813597-192813598
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1070909	0.87[EUR][1000 genomes]
rs1152746	0.89[EUR][1000 genomes]
rs1231727	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231728	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1231729	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1231730	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231731	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231732	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231733	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231734	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231735	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1231736	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1231737	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231738	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1231739	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231740	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231741	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231742	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1231744	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1231746	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1231747	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1231749	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1231750	0.82[EUR][1000 genomes]
rs1231751	0.92[EUR][1000 genomes]
rs1231754	0.91[EUR][1000 genomes]
rs1231757	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1231758	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1231759	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1231760	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1231762	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1231763	0.83[EUR][1000 genomes]
rs1231764	0.83[EUR][1000 genomes]
rs1231765	0.83[EUR][1000 genomes]
rs1231766	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1231767	0.89[EUR][1000 genomes]
rs1234722	0.82[EUR][1000 genomes]
rs1234723	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1237767	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12733094	0.89[EUR][1000 genomes]
rs12756953	0.86[EUR][1000 genomes]
rs1535034	0.83[EUR][1000 genomes]
rs16834948	0.89[EUR][1000 genomes]
rs17590238	0.88[EUR][1000 genomes]
rs1890973	0.88[EUR][1000 genomes]
rs2473740	0.82[EUR][1000 genomes]
rs2473741	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2473742	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2473744	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2473745	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2487284	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2487286	0.88[EUR][1000 genomes]
rs2487288	0.82[EUR][1000 genomes]
rs2746068	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2797395	0.82[EUR][1000 genomes]
rs34120198	0.87[EUR][1000 genomes]
rs34732347	0.87[EUR][1000 genomes]
rs34838432	0.88[EUR][1000 genomes]
rs34867585	0.87[EUR][1000 genomes]
rs35997646	0.87[EUR][1000 genomes]
rs36005848	0.87[EUR][1000 genomes]
rs4332340	0.89[EUR][1000 genomes]
rs4658075	0.88[EUR][1000 genomes]
rs56155184	0.89[EUR][1000 genomes]
rs58739396	0.87[EUR][1000 genomes]
rs60382150	0.88[EUR][1000 genomes]
rs6686024	0.88[EUR][1000 genomes]
rs6692203	0.89[EUR][1000 genomes]
rs710142	0.89[EUR][1000 genomes]
rs710144	0.98[EUR][1000 genomes]
rs710145	0.97[EUR][1000 genomes]
rs710146	0.97[EUR][1000 genomes]
rs842922	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs842923	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs842924	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs844529	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs859888	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs859890	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs863604	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 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	chr1:192807200-192816000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:192810000-192816000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:192811400-192816000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:192812000-192814400	Weak transcription	Aorta	Aorta
5	chr1:192812000-192816000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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