Variant report

Variant	rs59705032
Chromosome Location	chr15:42793643-42793644
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:42786349..42789071-chr15:42793305..42795618,2	K562	blood:
2	chr15:42786351..42790033-chr15:42790160..42794805,5	K562	blood:
3	chr15:42792525..42795008-chr15:42866851..42868814,2	K562	blood:

Variant related genes	Relation type
ENSG00000159433	Chromatin interaction
ENSG00000092531	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10518766	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1060291	1.00[ASN][1000 genomes]
rs1060293	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11022	1.00[ASN][1000 genomes]
rs11070376	1.00[ASN][1000 genomes]
rs11636577	1.00[ASN][1000 genomes]
rs16973320	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17709180	1.00[ASN][1000 genomes]
rs17709377	1.00[ASN][1000 genomes]
rs17766532	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1900921	1.00[ASN][1000 genomes]
rs2899051	1.00[ASN][1000 genomes]
rs2899059	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34359922	1.00[ASN][1000 genomes]
rs34643746	1.00[ASN][1000 genomes]
rs34792942	1.00[ASN][1000 genomes]
rs3986280	1.00[ASN][1000 genomes]
rs4923948	1.00[ASN][1000 genomes]
rs4924684	1.00[ASN][1000 genomes]
rs4924687	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56357092	1.00[ASN][1000 genomes]
rs56982416	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58042601	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58641431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59697584	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60380503	1.00[ASN][1000 genomes]
rs60584955	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60812675	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61489160	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022317	1.00[ASN][1000 genomes]
rs7180483	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402783	1.00[ASN][1000 genomes]
rs73402785	1.00[ASN][1000 genomes]
rs73404714	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73404717	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73404723	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73404730	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73404763	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73406518	1.00[ASN][1000 genomes]
rs73406534	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73406545	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74009095	1.00[ASN][1000 genomes]
rs8033412	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3334708	chr15:42664344-42827738	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv528725	chr15:42755555-43104406	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42788400-42808000	Weak transcription	Esophagus	oesophagus
2	chr15:42788600-42798400	Weak transcription	Ovary	ovary
3	chr15:42788600-42805600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr15:42788600-42806600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:42788600-42807200	Weak transcription	Fetal Kidney	kidney
6	chr15:42788800-42797000	Weak transcription	HSMMtube	muscle
7	chr15:42788800-42800400	Weak transcription	Fetal Lung	lung
8	chr15:42788800-42805200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr15:42788800-42805400	Weak transcription	Brain Germinal Matrix	brain
10	chr15:42789000-42794000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:42789000-42797000	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr15:42789000-42797000	Weak transcription	Brain Angular Gyrus	brain
13	chr15:42789000-42803400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:42789000-42805400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr15:42789000-42806400	Weak transcription	Thymus	Thymus
16	chr15:42789200-42794000	Enhancers	Placenta	Placenta
17	chr15:42789200-42796800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr15:42789200-42798400	Weak transcription	Primary T cells from cord blood	blood
19	chr15:42789200-42800600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:42789200-42802400	Weak transcription	Fetal Brain Female	brain
21	chr15:42789200-42804400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr15:42789200-42805800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr15:42789200-42806600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr15:42789600-42793800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr15:42790200-42793800	Strong transcription	Fetal Stomach	stomach
26	chr15:42790200-42793800	Enhancers	Pancreas	Pancrea
27	chr15:42790200-42794200	Enhancers	Adipose Nuclei	Adipose
28	chr15:42790400-42802600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr15:42790600-42797200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr15:42790600-42800200	Weak transcription	Psoas Muscle	Psoas
31	chr15:42790600-42805200	Weak transcription	Dnd41	blood
32	chr15:42790600-42806600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr15:42790600-42807200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr15:42790800-42794000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr15:42790800-42795800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:42790800-42797200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr15:42790800-42798400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr15:42790800-42805000	Weak transcription	Fetal Thymus	thymus
39	chr15:42790800-42809800	Weak transcription	Spleen	Spleen
40	chr15:42790800-42810000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr15:42790800-42821400	Weak transcription	Right Ventricle	heart
42	chr15:42791000-42794200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr15:42791200-42796800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr15:42791200-42803800	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr15:42791200-42809800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:42791400-42794000	Genic enhancers	Primary B cells from peripheral blood	blood
47	chr15:42791400-42796600	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr15:42791800-42796800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr15:42791800-42796800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr15:42792000-42793800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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