Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:133018589-133018855	IMR90	lung:	n/a	chr6:133018702-133018713 chr6:133018700-133018711 chr6:133018700-133018713 chr6:133018700-133018713 chr6:133018702-133018711
2	CEBPB	chr6:133018502-133018837	K562	blood:	n/a	chr6:133018702-133018713 chr6:133018700-133018711 chr6:133018700-133018713 chr6:133018700-133018713 chr6:133018702-133018711
3	CEBPB	chr6:133018611-133018838	HepG2	liver:	n/a	chr6:133018702-133018713 chr6:133018700-133018711 chr6:133018700-133018713 chr6:133018700-133018713 chr6:133018702-133018711

Variant related genes	Relation type
CCNG1P1	TF binding region

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

rs_ID	r²[population]
rs12524890	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12527885	0.80[AMR][1000 genomes]
rs12529776	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12661455	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12661928	0.91[ASN][1000 genomes]
rs12661954	0.93[ASN][1000 genomes]
rs12662444	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12663513	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12664412	0.91[ASN][1000 genomes]
rs12665089	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17061677	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2206566	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2223612	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3798795	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3798797	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs45461891	0.84[AMR][1000 genomes]
rs45511792	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs45568334	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56898355	0.86[ASN][1000 genomes]
rs58694797	0.86[ASN][1000 genomes]
rs73546608	0.80[AMR][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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133015200-133019400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:133015200-133019800	Weak transcription	Stomach Mucosa	stomach
3	chr6:133015400-133021200	Strong transcription	Liver	Liver
4	chr6:133017800-133032200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr6:133018000-133020000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr6:133018200-133028400	Weak transcription	Primary monocytes fromperipheralblood	blood

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