Variant report

No.	Distal block	Cell Line	Cell type
1	chr14:70195404..70198253-chr14:70727101..70728631,2	MCF-7	breast:
2	chr14:70194965..70197574-chr14:70237886..70240274,2	MCF-7	breast:
3	chr14:70050809..70053734-chr14:70194375..70196806,2	K562	blood:
4	chr14:70195248..70198988-chr14:70201420..70203953,3	K562	blood:

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11620826	0.80[EUR][1000 genomes]
rs11622083	0.92[ASN][1000 genomes]
rs11622092	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11623812	0.80[EUR][1000 genomes]
rs11624654	0.93[ASN][1000 genomes]
rs11624754	0.93[ASN][1000 genomes]
rs11627867	0.80[EUR][1000 genomes]
rs11629212	0.80[EUR][1000 genomes]
rs12587433	0.80[EUR][1000 genomes]
rs12589061	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17107177	0.80[EUR][1000 genomes]
rs2275124	0.80[EUR][1000 genomes]
rs2332163	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2332165	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3784143	0.80[EUR][1000 genomes]
rs3784144	0.80[EUR][1000 genomes]
rs3784149	0.80[EUR][1000 genomes]
rs3825736	0.80[EUR][1000 genomes]
rs4902742	0.85[EUR][1000 genomes]
rs55654254	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56325932	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57016627	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57346352	0.92[ASN][1000 genomes]
rs61980727	0.80[EUR][1000 genomes]
rs61980737	0.80[EUR][1000 genomes]
rs61982060	0.80[EUR][1000 genomes]
rs61982061	0.80[EUR][1000 genomes]
rs61982064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61982066	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8010776	0.80[EUR][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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70194000-70196600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr14:70194000-70196800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr14:70194000-70199200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:70194200-70197600	Weak transcription	Liver	Liver
5	chr14:70194200-70197800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr14:70194200-70200400	Weak transcription	Esophagus	oesophagus
7	chr14:70194400-70197800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:70194400-70197800	Weak transcription	Hela-S3	cervix
9	chr14:70195200-70196400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr14:70195600-70196400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr14:70195800-70196400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr14:70195800-70196600	Weak transcription	Left Ventricle	heart
13	chr14:70195800-70196600	Weak transcription	K562	blood

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