Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:91579267..91582285-chr13:91588672..91590280,3	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10507988	1.00[EUR][1000 genomes]
rs11841091	1.00[EUR][1000 genomes]
rs11841369	1.00[EUR][1000 genomes]
rs11842059	1.00[EUR][1000 genomes]
rs1335559	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1470771	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1470772	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16944862	1.00[EUR][1000 genomes]
rs16944890	1.00[EUR][1000 genomes]
rs16944919	1.00[EUR][1000 genomes]
rs16944928	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs16944959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16944982	0.85[AFR][1000 genomes]
rs16952565	1.00[EUR][1000 genomes]
rs17842723	0.83[EUR][1000 genomes]
rs41275862	1.00[EUR][1000 genomes]
rs58748013	0.84[AFR][1000 genomes]
rs73599262	1.00[EUR][1000 genomes]
rs73599266	1.00[EUR][1000 genomes]
rs73599275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73599282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73599290	0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948709	chr13:90753085-91745571	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv932206	chr13:91370888-91878374	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
4	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 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	chr13:91559600-91581000	Weak transcription	Right Atrium	heart
2	chr13:91578800-91585200	Weak transcription	A549	lung
3	chr13:91579200-91580600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:91579400-91582800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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