Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67852630..67855318-chr2:67906179..67908434,2	K562	blood:

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

rs_ID	r²[population]
rs10194853	0.81[AMR][1000 genomes]
rs10496148	0.90[EUR][1000 genomes]
rs11126148	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12162351	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12465119	0.86[ASN][1000 genomes]
rs1430762	0.81[AMR][1000 genomes]
rs17034087	0.83[AMR][1000 genomes]
rs17034097	0.81[AMR][1000 genomes]
rs17034147	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17034224	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17040171	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2195683	0.91[EUR][1000 genomes]
rs2195684	0.91[EUR][1000 genomes]
rs2861712	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58113451	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60157569	0.88[EUR][1000 genomes]
rs60205859	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72621576	0.88[AFR][1000 genomes]
rs72621582	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72621584	0.81[AMR][1000 genomes]
rs72621585	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72621587	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72621588	0.99[ASN][1000 genomes]
rs72621591	0.88[EUR][1000 genomes]
rs72621593	0.88[EUR][1000 genomes]
rs72621594	0.88[EUR][1000 genomes]
rs72621595	0.88[EUR][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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv1007345	chr2:67870225-67980094	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv834250	chr2:67897722-68051532	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67903600-67912200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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