Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103506208..103509003-chr7:103526109..103528413,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10226733	0.81[ASN][1000 genomes]
rs10227303	1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs10227818	0.83[ASN][1000 genomes]
rs10228185	0.83[ASN][1000 genomes]
rs10231740	0.83[ASN][1000 genomes]
rs10257331	0.83[ASN][1000 genomes]
rs10257449	0.83[ASN][1000 genomes]
rs10270408	0.81[ASN][1000 genomes]
rs12667097	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17156555	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17157010	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17157043	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17157057	0.87[ASN][1000 genomes]
rs17157072	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17157084	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17157104	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17157114	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35734631	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6979556	0.83[ASN][1000 genomes]
rs73712281	0.82[ASN][1000 genomes]
rs73712282	0.83[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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103520800-103529200	Weak transcription	HepG2	liver
2	chr7:103524200-103526800	Weak transcription	K562	blood
3	chr7:103526400-103527400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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