Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:121500985..121503784-chr7:121505608..121507166,2	K562	blood:

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

rs_ID	r²[population]
rs10953948	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11543745	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12669706	0.94[JPT][hapmap]
rs12671267	0.83[EUR][1000 genomes]
rs12672519	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12673871	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16870718	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1916885	0.94[JPT][hapmap]
rs2191783	0.94[JPT][hapmap]
rs35807933	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3757551	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3801374	0.80[AMR][1000 genomes]
rs3801377	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3801380	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58748383	0.80[ASN][1000 genomes]
rs6965735	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6971645	0.81[CEU][hapmap];0.94[JPT][hapmap]
rs73717719	0.83[EUR][1000 genomes]
rs740965	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7797043	0.98[ASN][1000 genomes]
rs9641678	0.81[CEU][hapmap];0.94[JPT][hapmap]

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	nsv429808	chr7:121384049-121600049	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1802911	chr7:121489994-121524500	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1798234	chr7:121494164-121505847	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121500800-121512800	Weak transcription	Aorta	Aorta
2	chr7:121504000-121508400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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