Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:58539325..58541769-chr1:58543438..58546362,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10889083	0.86[ASN][1000 genomes]
rs10889084	0.83[CHB][hapmap]
rs1106367	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs12031853	0.83[CHB][hapmap]
rs12041539	0.90[JPT][hapmap]
rs12058945	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs1213764	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs1213770	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs1213771	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs1320555	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs1359495	0.96[CHB][hapmap]
rs17116867	0.91[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs2764685	0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2764686	0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2764687	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2806406	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs3118212	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3121907	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58029039	0.85[ASN][1000 genomes]
rs59081310	0.85[ASN][1000 genomes]
rs7522031	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs821525	0.84[ASN][1000 genomes]
rs821526	0.84[ASN][1000 genomes]
rs821527	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs821528	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs946310	0.91[CHB][hapmap];0.84[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58539000-58543000	Enhancers	Fetal Brain Male	brain
2	chr1:58539600-58541000	Weak transcription	Fetal Brain Female	brain

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