Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:33463213..33467360-chr6:33468926..33472563,4	K562	blood:
2	chr6:33463213..33466886-chr6:33468926..33471484,3	K562	blood:
3	chr6:33396539..33398732-chr6:33463165..33465539,2	K562	blood:

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11963294	1.00[CHB][hapmap]
rs12529825	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1536042	1.00[JPT][hapmap]
rs16869178	1.00[JPT][hapmap]
rs1755038	0.84[EUR][1000 genomes]
rs2395451	1.00[JPT][hapmap]
rs34897283	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843520	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3843521	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3857558	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs449978	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs4711333	1.00[JPT][hapmap]
rs4713630	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4713631	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4713633	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4713647	1.00[JPT][hapmap]
rs480568	1.00[JPT][hapmap]
rs485623	1.00[JPT][hapmap]
rs557559	1.00[JPT][hapmap]
rs560218	1.00[JPT][hapmap]
rs561276	1.00[JPT][hapmap]
rs6457728	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6910219	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6910721	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs6913018	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7383692	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7752930	1.00[JPT][hapmap]
rs7757722	1.00[JPT][hapmap]
rs7762843	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes]
rs9368764	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9368765	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9368766	0.94[AMR][1000 genomes];0.97[EUR][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	nsv830637	chr6:33329365-33510704	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv602832	chr6:33382241-33520221	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 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	chr6:33453000-33474000	Weak transcription	Right Atrium	heart

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