Variant report

Variant	rs59357310
Chromosome Location	chr15:52862556-52862557
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HCFC1	chr15:52859032-52862695	Hela-S3	cervix:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52819294..52821098-chr15:52860363..52863142,2	MCF-7	breast:
2	chr15:52820217..52824623-chr15:52859000..52863588,7	MCF-7	breast:
3	chr15:52860513..52862699-chr15:55611421..55613423,2	K562	blood:
4	chr15:52861113..52864029-chr15:52869389..52871749,2	MCF-7	breast:
5	chr15:52585776..52589284-chr15:52859101..52864638,8	MCF-7	breast:
6	chr15:52860624..52863136-chr16:11348731..11351355,2	MCF-7	breast:
7	chr15:52861240..52863531-chr15:52869208..52872157,2	K562	blood:
8	chr15:52859855..52863944-chr15:52968349..52971887,6	MCF-7	breast:
9	chr15:52855349..52864927-chr15:52966670..52972620,15	MCF-7	breast:

No data

Variant related genes	Relation type
ARPP19	TF binding region
ENSG00000197535	Chromatin interaction
ENSG00000185338	Chromatin interaction
ENSG00000047346	Chromatin interaction
ENSG00000069943	Chromatin interaction
ENSG00000128833	Chromatin interaction
ENSG00000260618	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73396742	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471245	chr15:52607262-53187165	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv1041421	chr15:52661342-53148286	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	esv1832020	chr15:52702400-52901914	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1047775	chr15:52822050-52912228	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv833006	chr15:52825954-53040462	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52861200-52925200	Weak transcription	Stomach Mucosa	stomach
2	chr15:52861400-52873600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:52861400-52878600	Weak transcription	Ovary	ovary
4	chr15:52861400-52883600	Weak transcription	Lung	lung
5	chr15:52861600-52862800	Enhancers	HUVEC	blood vessel
6	chr15:52861600-52868600	Weak transcription	HSMMtube	muscle
7	chr15:52861600-52869800	Weak transcription	Primary B cells from cord blood	blood
8	chr15:52861600-52871200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:52861600-52871800	Weak transcription	Primary T cells from cord blood	blood
10	chr15:52861600-52872000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:52861600-52872000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:52861600-52872000	Weak transcription	Left Ventricle	heart
13	chr15:52861600-52872400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr15:52861600-52873000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr15:52861600-52873200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr15:52861600-52873600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:52861600-52874000	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr15:52861600-52880600	Weak transcription	Fetal Intestine Small	intestine
19	chr15:52861600-52883800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr15:52861600-52884000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr15:52861600-52885000	Weak transcription	Spleen	Spleen
22	chr15:52861600-52901600	Weak transcription	Esophagus	oesophagus
23	chr15:52861800-52862600	Weak transcription	Fetal Lung	lung
24	chr15:52861800-52863200	Weak transcription	HepG2	liver
25	chr15:52861800-52870800	Weak transcription	Primary B cells from peripheral blood	blood
26	chr15:52861800-52871800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr15:52861800-52872200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:52861800-52872200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:52861800-52872200	Weak transcription	Liver	Liver
30	chr15:52861800-52872200	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr15:52861800-52872400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr15:52861800-52873000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:52861800-52873000	Weak transcription	Placenta	Placenta
34	chr15:52861800-52873200	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr15:52861800-52873200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr15:52861800-52873400	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr15:52861800-52873600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr15:52861800-52873600	Weak transcription	Adipose Nuclei	Adipose
39	chr15:52861800-52873600	Weak transcription	Brain Anterior Caudate	brain
40	chr15:52861800-52873600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr15:52861800-52873600	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr15:52861800-52873800	Weak transcription	Fetal Thymus	thymus
43	chr15:52861800-52873800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr15:52861800-52874200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr15:52861800-52874200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:52861800-52874200	Weak transcription	Fetal Intestine Large	intestine
47	chr15:52861800-52874200	Weak transcription	Fetal Muscle Leg	muscle
48	chr15:52861800-52874200	Weak transcription	HSMM	muscle
49	chr15:52861800-52875000	Weak transcription	Brain Hippocampus Middle	brain
50	chr15:52861800-52875400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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