Variant report

No.	Distal block	Cell Line	Cell type
1	chr2:58935937..58937842-chr2:58949736..58951617,2	K562	blood:
2	chr2:58926366..58928682-chr2:58934169..58936932,2	K562	blood:
3	chr2:58935718..58937483-chr2:58954738..58957227,2	K562	blood:
4	chr2:58786984..58789724-chr2:58935931..58938374,2	MCF-7	breast:

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

rs_ID	r²[population]
rs1014585	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1158041	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11682437	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11693731	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12463832	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13025286	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1861410	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1922778	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1922779	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1922782	0.90[ASN][1000 genomes]
rs35881094	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4541244	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4672257	0.91[ASN][1000 genomes]
rs741310	0.84[EUR][1000 genomes]
rs7572888	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7582485	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7586515	0.81[AFR][1000 genomes]
rs7591382	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7591633	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7598875	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431180	chr2:58857542-59178687	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:58934800-58937200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:58935600-58937400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:58935600-58937800	Enhancers	K562	blood
4	chr2:58936000-58937000	Weak transcription	Fetal Brain Female	brain

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