Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:103874211..103876733-chr8:104025431..104027243,2	MCF-7	breast:
2	chr8:104025781..104028424-chr8:104031631..104033498,3	MCF-7	breast:
3	chr8:104020093..104022947-chr8:104025466..104027135,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1512348	0.82[YRI][hapmap]
rs16869978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16870018	1.00[CEU][hapmap];0.91[JPT][hapmap];0.96[EUR][1000 genomes]
rs16870020	0.85[YRI][hapmap]
rs16870033	1.00[CEU][hapmap];0.91[JPT][hapmap];0.98[EUR][1000 genomes]
rs16870035	0.85[YRI][hapmap]
rs28372883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3018948	0.87[ASN][1000 genomes]
rs3824225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3824228	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs486506	0.83[ASN][1000 genomes]
rs488420	0.83[ASN][1000 genomes]
rs575524	0.85[YRI][hapmap]
rs582100	0.82[YRI][hapmap]
rs60356223	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs613121	0.80[ASN][1000 genomes]
rs615348	0.80[ASN][1000 genomes]
rs62525309	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525313	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62525314	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62525315	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62525329	0.94[EUR][1000 genomes]
rs628793	0.83[ASN][1000 genomes]
rs630236	0.83[ASN][1000 genomes]
rs631019	0.83[ASN][1000 genomes]
rs642994	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs644305	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	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104023200-104032000	Weak transcription	K562	blood
2	chr8:104023200-104032800	Weak transcription	Pancreas	Pancrea
3	chr8:104026600-104032000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:104027000-104027400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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