Variant report

Variant	nsv182603
Chromosome Location	chr20:25507012-25507013
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	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:

Extended variants
information (count: 2 )
Associated
traits (count: 56 )

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	rs377090417	chr20:25507012-25507013	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs369694432	chr20:25507013-25507014	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25493200-25512800	Weak transcription	Colon Smooth Muscle	Colon
2	chr20:25493600-25513000	Weak transcription	Left Ventricle	heart
3	chr20:25495800-25519400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr20:25496000-25512400	Weak transcription	Brain Angular Gyrus	brain
5	chr20:25496000-25513200	Weak transcription	HUVEC	blood vessel
6	chr20:25497400-25512400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr20:25497400-25512400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr20:25497400-25514800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr20:25497600-25507200	Weak transcription	Colonic Mucosa	Colon
10	chr20:25497600-25512600	Weak transcription	Fetal Heart	heart
11	chr20:25497800-25512200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr20:25498000-25511000	Weak transcription	Brain Hippocampus Middle	brain
13	chr20:25498200-25510800	Weak transcription	Brain Substantia Nigra	brain
14	chr20:25498200-25512200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr20:25498200-25512200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr20:25498200-25512600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr20:25498200-25512600	Weak transcription	Brain Anterior Caudate	brain
18	chr20:25498200-25512800	Weak transcription	Adipose Nuclei	Adipose
19	chr20:25498200-25513000	Weak transcription	Fetal Thymus	thymus
20	chr20:25498200-25514600	Weak transcription	Pancreas	Pancrea
21	chr20:25498200-25519000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr20:25498200-25519400	Weak transcription	Gastric	stomach
23	chr20:25498200-25532200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr20:25498400-25519200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr20:25498600-25512800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr20:25501200-25507200	Strong transcription	Fetal Lung	lung
27	chr20:25501600-25507200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr20:25502000-25507200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr20:25502000-25507600	Strong transcription	Dnd41	blood
30	chr20:25502400-25507200	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr20:25502400-25507200	Strong transcription	Brain Germinal Matrix	brain
32	chr20:25502400-25507200	Strong transcription	Fetal Muscle Leg	muscle
33	chr20:25502600-25519800	Weak transcription	Stomach Mucosa	stomach
34	chr20:25502800-25513200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr20:25503000-25507400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr20:25503400-25507400	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr20:25503400-25507400	Strong transcription	Thymus	Thymus
38	chr20:25503400-25508800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:25503400-25512400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr20:25504000-25507600	Strong transcription	Fetal Stomach	stomach
41	chr20:25504400-25507200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr20:25504400-25507400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr20:25504800-25507200	Strong transcription	Stomach Smooth Muscle	stomach
44	chr20:25504800-25508200	Weak transcription	Placenta	Placenta
45	chr20:25504800-25512800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr20:25505000-25507400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr20:25505000-25512800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr20:25505200-25507600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr20:25505200-25507600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr20:25505200-25512800	Weak transcription	Esophagus	oesophagus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links