Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1155492	0.81[ASN][1000 genomes]
rs1323819	0.82[AFR][1000 genomes]
rs1323820	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1323821	0.81[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1323824	0.82[AFR][1000 genomes]
rs1323827	0.89[ASN][1000 genomes]
rs1886140	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2406280	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2406282	0.89[ASN][1000 genomes]
rs3118053	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3118054	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3118055	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3118057	0.89[ASN][1000 genomes]
rs3118058	0.89[ASN][1000 genomes]
rs3118059	0.81[ASN][1000 genomes]
rs3131736	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3131737	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3131738	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3131740	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3131741	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3131742	0.89[ASN][1000 genomes]
rs3131743	0.80[ASN][1000 genomes]
rs3131745	0.89[ASN][1000 genomes]
rs927612	0.89[ASN][1000 genomes]
rs978786	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr1:58222400-58232800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:58226400-58227800	Enhancers	Fetal Heart	heart
3	chr1:58226600-58227800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:58226800-58227600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:58227000-58227600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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