Variant report

No.	Distal block	Cell Line	Cell type
1	chr2:205262660..205264266-chr2:205270395..205272179,2	K562	blood:
2	chr2:205269954..205272543-chr2:205315221..205317326,2	K562	blood:
3	chr2:205266083..205268552-chr2:205270043..205272766,3	K562	blood:
4	chr2:205266871..205268427-chr2:205270043..205271674,2	K562	blood:
5	chr2:205268926..205271730-chr2:205279603..205282127,2	K562	blood:

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

rs_ID	r²[population]
rs10084407	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10177202	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11676622	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11690703	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11691106	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12615494	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs12694001	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13010387	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13413837	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13416642	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13419430	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1374710	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1374711	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34130978	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62177725	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62177726	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6712212	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67404857	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71408989	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7597728	0.89[AMR][1000 genomes];0.93[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	nsv875721	chr2:205232072-205306024	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:205267400-205272600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:205270600-205272600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:205270800-205271400	Weak transcription	K562	blood
4	chr2:205270800-205273000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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