Variant report

Variant	esv3388472
Chromosome Location	chr3:21923798-21923980
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	chr3:21922639..21924964-chr3:21928274..21929966,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139786984	chr3:21923818-21923819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147044873	chr3:21923830-21923831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs59982156	chr3:21923831-21923832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112819989	chr3:21923836-21923837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544197921	chr3:21923837-21923838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2673536	chr3:21923838-21923839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs187087895	chr3:21923853-21923854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192331983	chr3:21923865-21923866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560384389	chr3:21923867-21923868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13433703	chr3:21923870-21923871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2336513	chr3:21923872-21923873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183619075	chr3:21923879-21923880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537943278	chr3:21923903-21923904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71624342	chr3:21923914-21923915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2336514	chr3:21923915-21923916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377470056	chr3:21923916-21923917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143212522	chr3:21923925-21923926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146209990	chr3:21923936-21923937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112825632	chr3:21923943-21923944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540908230	chr3:21923955-21923956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374468761	chr3:21923958-21923959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139232998	chr3:21923976-21923977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21922000-21927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:21923600-21923800	Enhancers	Fetal Lung	lung

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