Variant report

Variant	rs72808977
Chromosome Location	chr5:115698365-115698366
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:115692236..115694986-chr5:115697167..115699493,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs17139524	0.87[ASN][1000 genomes]
rs17139532	0.91[ASN][1000 genomes]
rs17139604	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17139607	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55663230	0.88[ASN][1000 genomes]
rs55742067	0.81[ASN][1000 genomes]
rs55857351	1.00[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs56168251	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56317742	0.88[ASN][1000 genomes]
rs56370685	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs57209700	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57526524	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58291729	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58776100	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72804893	1.00[AFR][1000 genomes]
rs72804899	1.00[AFR][1000 genomes]
rs72806908	1.00[AFR][1000 genomes]
rs72806910	1.00[AFR][1000 genomes]
rs72806919	1.00[AFR][1000 genomes]
rs72806920	1.00[AFR][1000 genomes]
rs72806923	1.00[AFR][1000 genomes]
rs72808904	1.00[AFR][1000 genomes]
rs72808928	1.00[AFR][1000 genomes]
rs72808931	1.00[AFR][1000 genomes]
rs72808945	1.00[AFR][1000 genomes]
rs72808952	1.00[AFR][1000 genomes]
rs72808958	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs72808959	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs72808960	0.82[ASN][1000 genomes]
rs72808961	0.88[ASN][1000 genomes]
rs72808964	0.82[ASN][1000 genomes]
rs72808969	1.00[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs72808973	1.00[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs72808976	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72808978	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72808979	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72808981	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72808984	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72808985	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72808987	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72808989	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72808992	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34146	chr5:115315944-115729919	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	esv2755349	chr5:115384101-115733101	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv882746	chr5:115566026-115704566	Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1017983	chr5:115578765-115713688	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv4968	chr5:115635771-115714856	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv2763489	chr5:115693166-115733327	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2753353	chr5:115696118-115699265	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115684400-115705800	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr5:115685000-115721400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr5:115687200-115706400	Weak transcription	Liver	Liver
4	chr5:115694400-115707800	Weak transcription	Spleen	Spleen
5	chr5:115695200-115700000	Weak transcription	K562	blood
6	chr5:115695800-115706600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:115695800-115714600	Weak transcription	Thymus	Thymus
8	chr5:115696000-115708000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr5:115696400-115707600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr5:115696400-115708400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:115697000-115700600	Weak transcription	GM12878-XiMat	blood
12	chr5:115697600-115698400	Enhancers	Right Ventricle	heart
13	chr5:115697600-115699000	Strong transcription	Primary T cells from cord blood	blood
14	chr5:115697600-115700600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:115697600-115705400	Weak transcription	Left Ventricle	heart
16	chr5:115697600-115707400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr5:115697600-115708200	Weak transcription	Lung	lung
18	chr5:115697600-115712000	Weak transcription	Aorta	Aorta
19	chr5:115697600-115714000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:115697600-115748400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr5:115697800-115698400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr5:115697800-115699400	Strong transcription	Primary B cells from cord blood	blood
23	chr5:115697800-115706600	Weak transcription	Fetal Intestine Small	intestine
24	chr5:115697800-115706800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr5:115697800-115708200	Weak transcription	Psoas Muscle	Psoas
26	chr5:115697800-115708400	Weak transcription	Colonic Mucosa	Colon
27	chr5:115698000-115700800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr5:115698000-115722800	Weak transcription	Pancreas	Pancrea

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