Variant report

No.	Distal block	Cell Line	Cell type
1	chr20:57225277..57226150-chr8:91294237..91295072,2	MCF-7	breast:
2	chr8:91291547..91294986-chr8:91296579..91299012,3	MCF-7	breast:
3	chr8:91294512..91297405-chr8:91297809..91300397,3	MCF-7	breast:
4	chr8:91294194..91296983-chr8:91299273..91302205,2	MCF-7	breast:
5	chr8:91294415..91296685-chr8:91297719..91300044,3	K562	blood:
6	chr8:91289933..91292058-chr8:91293995..91295597,2	K562	blood:
7	chr8:91290558..91293429-chr8:91294097..91296686,3	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12544366	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12545140	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12546302	0.87[AMR][1000 genomes]
rs12547394	0.85[AMR][1000 genomes]
rs12549515	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12549630	0.85[AMR][1000 genomes]
rs12549660	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12550324	0.85[AMR][1000 genomes]
rs16904149	0.85[AMR][1000 genomes]
rs2189257	0.85[AMR][1000 genomes]
rs2285725	0.85[AMR][1000 genomes]
rs4735301	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59497517	0.87[AMR][1000 genomes]
rs6470854	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6470856	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7016389	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs72606647	0.87[AMR][1000 genomes]
rs72606648	0.87[AMR][1000 genomes]
rs72606649	0.85[AMR][1000 genomes]
rs72606650	0.85[AMR][1000 genomes]
rs72606651	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606652	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606653	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606654	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606655	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606656	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72606657	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs970473	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][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	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91292200-91296400	Weak transcription	K562	blood
2	chr8:91293600-91297200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr8:91293800-91297200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:91294200-91297000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr8:91294400-91297000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr8:91294400-91297000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:91294400-91297200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:91294600-91295000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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