Variant report

No.	Distal block	Cell Line	Cell type
1	chr4:85391036..85392035-chr4:85424665..85425609,5	K562	blood:
2	chr10:56063971..56064546-chr4:85391561..85392244,2	MCF-7	breast:
3	chr4:85391114..85392076-chr4:85425152..85425657,2	MCF-7	breast:
4	chr4:85391076..85391959-chr4:85424677..85425618,9	MCF-7	breast:
5	chr4:85389841..85391971-chr4:85396511..85399412,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10027841	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1037042	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13116689	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444954	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444958	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444959	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1562149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028764	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028766	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4693109	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4693682	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4693683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535536	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535537	1.00[ASN][1000 genomes]
rs895112	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895114	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs962304	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs972863	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs987949	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	nsv829997	chr4:85244076-85409405	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv829998	chr4:85299693-85473450	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85388600-85392600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:85389400-85394800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr4:85391400-85391800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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