Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:91011585..91013133-chr8:91244828..91247817,2	K562	blood:
2	chr8:91204703..91206737-chr8:91244479..91246995,2	K562	blood:

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

rs_ID	r²[population]
rs11776578	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11777851	1.00[ASN][1000 genomes]
rs11779938	1.00[ASN][1000 genomes]
rs11989856	1.00[ASN][1000 genomes]
rs12114040	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[ASN][1000 genomes]
rs12115012	0.85[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16904078	1.00[ASN][1000 genomes]
rs16904104	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap]
rs16904193	1.00[LWK][hapmap]
rs16904195	1.00[LWK][hapmap]
rs55641669	1.00[ASN][1000 genomes]
rs55642901	1.00[ASN][1000 genomes]
rs55899852	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56044560	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56400806	1.00[ASN][1000 genomes]
rs58912966	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs60226967	1.00[ASN][1000 genomes]
rs73695307	1.00[ASN][1000 genomes]
rs73695315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73695320	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73698034	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	esv3357030	chr8:91244726-91246674	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91243800-91248000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:91244800-91246800	Weak transcription	K562	blood

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