Variant report

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr13:50464632-50464749	MCF-7	breast:	n/a	n/a
2	TBP	chr13:50464720-50464745	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:50464730..50466250-chr14:39735376..39737030,2	MCF-7	breast:
2	chr13:50464224..50465231-chr14:39736139..39736859,3	MCF-7	breast:

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No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM13-8	chr13:50464545-50467516	NR_003268

No data

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11617416	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11620214	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61747167	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[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	esv3436655	chr13:50462077-50472044	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr13:50464600-50464800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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