Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:4646609..4648240-chr6:4675199..4677622,2	MCF-7	breast:
2	chr6:4671964..4676370-chr6:4676405..4678296,5	K562	blood:
3	chr6:4669229..4672483-chr6:4677301..4680282,4	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1040542	0.86[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1040543	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs13195286	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13215768	0.95[EUR][1000 genomes]
rs2073041	0.92[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs423699	0.95[EUR][1000 genomes]
rs440298	0.94[EUR][1000 genomes]
rs451971	0.95[EUR][1000 genomes]
rs4960015	0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs761180	0.93[EUR][1000 genomes]
rs761181	0.93[EUR][1000 genomes]
rs761182	0.94[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs7759755	0.87[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs9378898	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378899	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378900	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378901	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378902	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392060	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392621	0.98[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs9502221	0.94[ASN][1000 genomes]
rs9504195	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9504197	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[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	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv528627	chr6:4614058-4731340	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv883416	chr6:4666878-4690760	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4665000-4680400	Weak transcription	Right Atrium	heart
2	chr6:4669000-4695600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:4669400-4677600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr6:4673600-4677800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:4674200-4677600	Weak transcription	Placenta	Placenta
6	chr6:4675600-4684000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:4675800-4677600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:4676000-4677600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr6:4676200-4678800	Weak transcription	K562	blood
10	chr6:4677400-4678200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:4677400-4678200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:4677400-4678200	Enhancers	Esophagus	oesophagus

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