Variant report

Variant	esv3391315
Chromosome Location	chr3:179653633-179655806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187903407	chr3:179653651-179653652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559002321	chr3:179653658-179653659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192789614	chr3:179653729-179653730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184318081	chr3:179653763-179653764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564293264	chr3:179653767-179653768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533465078	chr3:179653777-179653778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550414772	chr3:179653818-179653819	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563551899	chr3:179653842-179653843	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556889935	chr3:179653864-179653865	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529264115	chr3:179653877-179653878	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549531197	chr3:179653878-179653879	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150126466	chr3:179653906-179653907	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534864653	chr3:179653936-179653937	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs80141180	chr3:179653987-179653988	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550486232	chr3:179653991-179653992	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575837821	chr3:179654002-179654003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12696482	chr3:179654084-179654085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs557194741	chr3:179654105-179654106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114727427	chr3:179654166-179654167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187950440	chr3:179654198-179654199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138449182	chr3:179654208-179654209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555419768	chr3:179654253-179654254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145804438	chr3:179654341-179654342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111797419	chr3:179654342-179654343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572607533	chr3:179654355-179654356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140256357	chr3:179654361-179654362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192325886	chr3:179654428-179654429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527800252	chr3:179654442-179654443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578101139	chr3:179654452-179654453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60214865	chr3:179654577-179654578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564355360	chr3:179654620-179654621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13325892	chr3:179654629-179654630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529308966	chr3:179654638-179654639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111376708	chr3:179654651-179654652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543043541	chr3:179654659-179654660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559740626	chr3:179654750-179654751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139030729	chr3:179654775-179654776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142216993	chr3:179654793-179654794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80001589	chr3:179654804-179654805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184384637	chr3:179654816-179654817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533503072	chr3:179654855-179654856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149871575	chr3:179654856-179654857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367700521	chr3:179654857-179654858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77954496	chr3:179654910-179654911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377272759	chr3:179654938-179654939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550635281	chr3:179654942-179654943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79115987	chr3:179654969-179654970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536095430	chr3:179655033-179655034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527936133	chr3:179655121-179655122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188816237	chr3:179655137-179655138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Esophageal squamous carcinoma	17470683	CNVD

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179644400-179660000	Weak transcription	Pancreas	Pancrea
2	chr3:179648400-179660000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:179652000-179655200	Weak transcription	Dnd41	blood
4	chr3:179652000-179660200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:179652400-179653800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:179653000-179659200	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:179653600-179660400	Weak transcription	Brain Substantia Nigra	brain
8	chr3:179653800-179654000	Genic enhancers	Brain Inferior Temporal Lobe	brain
9	chr3:179654000-179659800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:179655200-179655800	ZNF genes & repeats	Dnd41	blood
11	chr3:179655800-179656600	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links