Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:63950179..63953550-chr8:63956000..63961014,4	MCF-7	breast:
2	chr8:63949865..63952896-chr8:63955225..63959102,3	K562	blood:

Variant related genes	Relation type
ENSG00000137563	Chromatin interaction

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10094071	0.94[ASN][1000 genomes]
rs1031551	0.90[AFR][1000 genomes]
rs11545076	0.90[AFR][1000 genomes]
rs11988534	0.93[AFR][1000 genomes]
rs11989788	0.92[AFR][1000 genomes]
rs12682204	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13248452	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13267266	0.91[AFR][1000 genomes]
rs1800909	0.92[AFR][1000 genomes]
rs1963947	0.83[AFR][1000 genomes]
rs1963948	0.90[AFR][1000 genomes]
rs2353903	0.86[ASN][1000 genomes]
rs2736681	0.94[ASN][1000 genomes]
rs28816542	0.87[ASN][1000 genomes]
rs34099334	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34349258	0.88[AFR][1000 genomes]
rs34428496	0.90[AFR][1000 genomes]
rs34554414	0.87[AFR][1000 genomes]
rs34565227	0.87[AFR][1000 genomes]
rs35791650	0.83[AFR][1000 genomes]
rs3758149	0.92[AFR][1000 genomes]
rs3780126	0.93[ASN][1000 genomes]
rs4546655	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4739043	0.92[ASN][1000 genomes]
rs4739045	0.92[ASN][1000 genomes]
rs62510090	0.90[AFR][1000 genomes]
rs6472067	0.92[ASN][1000 genomes]
rs6472068	0.92[ASN][1000 genomes]
rs6472075	0.86[ASN][1000 genomes]
rs6996155	0.86[ASN][1000 genomes]
rs6996325	0.85[ASN][1000 genomes]
rs7001383	0.92[ASN][1000 genomes]
rs7004934	0.89[ASN][1000 genomes]
rs7005322	0.88[ASN][1000 genomes]
rs7007125	0.87[ASN][1000 genomes]
rs7386567	0.91[ASN][1000 genomes]
rs7830578	0.92[ASN][1000 genomes]
rs7832731	0.88[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	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv465701	chr8:63951237-64080486	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv611448	chr8:63951237-64080486	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12679179	GGH	cis	Adipose Subcutaneous	GTEx
rs12679179	GGH	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63956400-63958400	Weak transcription	Aorta	Aorta

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