Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:120404067..120405574-chr7:120407011..120408977,2	K562	blood:
2	chr7:120399996..120403218-chr7:120404535..120409322,5	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10245393	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10251949	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10256493	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10256716	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10272339	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10487403	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1468361	1.00[CHB][hapmap]
rs17142902	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17142908	1.00[CHB][hapmap]
rs17142964	1.00[ASN][1000 genomes]
rs17142967	1.00[ASN][1000 genomes]
rs17142974	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1859534	0.82[JPT][hapmap]
rs41424845	1.00[JPT][hapmap]
rs4730974	1.00[JPT][hapmap]
rs6466755	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6944490	1.00[CHB][hapmap]
rs6977602	0.81[ASN][1000 genomes]
rs73425840	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7777916	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7790895	1.00[JPT][hapmap]
rs7792191	0.85[YRI][hapmap]
rs7795370	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7806523	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7807447	0.85[YRI][hapmap]
rs7812111	1.00[JPT][hapmap]

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	esv1818826	chr7:120405335-120622836	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr7:120407000-120414600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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