Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:58944012..58945582-chr2:58954897..58957559,2	K562	blood:
2	chr2:58935718..58937483-chr2:58954738..58957227,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10176091	0.80[ASN][1000 genomes]
rs10207788	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10211534	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10865309	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12475168	0.85[ASN][1000 genomes]
rs12613375	0.85[ASN][1000 genomes]
rs12619538	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12622165	0.83[ASN][1000 genomes]
rs13416859	0.90[ASN][1000 genomes]
rs13417036	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13428870	0.89[ASN][1000 genomes]
rs1641155	0.86[ASN][1000 genomes]
rs17049705	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17049709	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17049712	0.89[ASN][1000 genomes]
rs17049722	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17615494	0.90[ASN][1000 genomes]
rs1796435	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2540324	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2540325	0.94[ASN][1000 genomes]
rs2708146	0.88[ASN][1000 genomes]
rs55767040	0.90[ASN][1000 genomes]
rs62142340	0.99[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62142342	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62144560	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6722165	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6741951	0.89[ASN][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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58948400-58955200	Weak transcription	K562	blood
2	chr2:58948400-58960000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:58953600-58958000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:58954200-58958600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:58954600-58963200	Enhancers	Primary hematopoietic stem cells	blood

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