Variant report

Variant	nsv569965
Chromosome Location	chr15:73660457-73661071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:73659851..73663146-chr15:73925069..73927598,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPTN-2	chr15:73660613-73661255	NONHSAT047146

Variant related genes	Relation type
ENSG00000156642	chromatin interactions

Extended variants
information (count: 10 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143090627	chr15:73660505-73660506	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376849038	chr15:73660564-73660565	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201193660	chr15:73660576-73660577	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547829940	chr15:73660645-73660646	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs566095713	chr15:73660741-73660742	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs536621293	chr15:73660781-73660782	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs548581131	chr15:73660800-73660801	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs577671006	chr15:73660879-73660880	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs183675842	chr15:73661018-73661019	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs537745479	chr15:73661047-73661048	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73658600-73661800	Active TSS	Right Atrium	heart
2	chr15:73659000-73660600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:73659200-73660600	Bivalent Enhancer	Lung	lung
4	chr15:73659200-73661400	Active TSS	Left Ventricle	heart
5	chr15:73659200-73661600	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr15:73659200-73661800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
7	chr15:73659200-73662000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:73659400-73661200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
9	chr15:73659400-73661400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
10	chr15:73659400-73661800	Bivalent Enhancer	Spleen	Spleen
11	chr15:73659400-73662000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr15:73659400-73662000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr15:73659400-73662200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr15:73659400-73662200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr15:73659600-73661400	Flanking Active TSS	Pancreas	Pancrea
16	chr15:73659600-73661800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:73659600-73662200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr15:73659600-73662200	Bivalent/Poised TSS	Fetal Brain Female	brain
19	chr15:73659800-73661000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
20	chr15:73659800-73661200	Enhancers	Liver	Liver
21	chr15:73659800-73661400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:73659800-73661600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr15:73659800-73661800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr15:73659800-73662000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr15:73660000-73661200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
26	chr15:73660000-73661200	Flanking Active TSS	Stomach Smooth Muscle	stomach
27	chr15:73660000-73661400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:73660000-73661400	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:73660000-73661400	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr15:73660000-73661400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
31	chr15:73660000-73661400	Weak transcription	Fetal Heart	heart
32	chr15:73660000-73661800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr15:73660000-73661800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:73660000-73661800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr15:73660000-73662200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
36	chr15:73660000-73662200	Active TSS	H9 Cell Line	embryonic stem cell
37	chr15:73660200-73660600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:73660200-73660800	Bivalent Enhancer	Esophagus	oesophagus
39	chr15:73660200-73661000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:73660200-73661200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr15:73660200-73661200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr15:73660200-73661200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:73660200-73661200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
44	chr15:73660200-73661200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
45	chr15:73660200-73661200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
46	chr15:73660200-73661200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
47	chr15:73660200-73661200	Flanking Bivalent TSS/Enh	HMEC	breast
48	chr15:73660200-73661400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:73660200-73661400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:73660200-73661400	Active TSS	Aorta	Aorta

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