Variant report

Variant	nsv1009557
Chromosome Location	chr2:51077569-51207542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
6	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
7	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
8	CEBPB	chr2:51184080-51184410	A549	lung:	n/a	chr2:51184131-51184142
9	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:51179690-51180699	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
12	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
14	CEBPB	chr2:51196168-51196459	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:51185072-51185406	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
16	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
18	CEBPB	chr2:51185052-51185376	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
19	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
20	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
21	CEBPB	chr2:51180081-51180588	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
22	CEBPB	chr2:51180165-51180469	A549	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
23	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
24	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
26	CEBPB	chr2:51185063-51185361	K562	blood:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
27	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
28	CEBPB	chr2:51184978-51185335	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
29	CEBPB	chr2:51184010-51184263	HepG2	liver:	n/a	chr2:51184131-51184142
30	CEBPB	chr2:51185035-51185357	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
31	CEBPB	chr2:51185020-51185401	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
32	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
33	CEBPB	chr2:51196130-51196480	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:51185019-51185391	H1-hESC	embryonic stem cell:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
35	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
36	CEBPB	chr2:51185008-51185377	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
37	CEBPB	chr2:51185005-51185419	IMR90	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
38	CEBPB	chr2:51185053-51185350	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
39	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
41	CEBPB	chr2:51185077-51185269	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185201-51185210 chr2:51185201-51185210
42	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
43	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
44	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
45	CEBPB	chr2:51196305-51196335	K562	blood:	n/a	n/a
46	CEBPB	chr2:51185039-51185390	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
47	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
49	CEBPB	chr2:51179722-51180770	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
50	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048

No.	Distal block	Cell Line	Cell type
1	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
2	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
3	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
4	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
5	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
6	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
7	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
8	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
9	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
10	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
11	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
12	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
13	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region

Extended variants
information (count: 4980 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4980 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17569963	chr2:51077569-51077570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571243367	chr2:51077585-51077586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192105303	chr2:51077623-51077624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143465797	chr2:51077624-51077625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72891307	chr2:51077645-51077646	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs534187331	chr2:51077681-51077682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555661998	chr2:51077772-51077773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185085607	chr2:51077773-51077774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72838782	chr2:51077793-51077794	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs66912589	chr2:51077881-51077882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575542253	chr2:51077882-51077883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562942671	chr2:51077889-51077890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs398060178	chr2:51077890-51077891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35938221	chr2:51077908-51077909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199575763	chr2:51077909-51077910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578032592	chr2:51078049-51078050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189462390	chr2:51078107-51078108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2882927	chr2:51078112-51078113	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527501587	chr2:51078130-51078131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549248553	chr2:51078138-51078139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561173147	chr2:51078140-51078141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531675475	chr2:51078189-51078190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368458106	chr2:51078235-51078236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180899868	chr2:51078266-51078267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538339323	chr2:51078321-51078322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367681330	chr2:51078380-51078381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566697195	chr2:51078387-51078388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546834214	chr2:51078436-51078437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs41422052	chr2:51078447-51078448	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs185807929	chr2:51078530-51078531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79735006	chr2:51078601-51078602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556264294	chr2:51078618-51078619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577998618	chr2:51078644-51078645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545141154	chr2:51078708-51078709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374600242	chr2:51078719-51078720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572227169	chr2:51078751-51078752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200065722	chr2:51078752-51078753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542831399	chr2:51078770-51078771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561111736	chr2:51078776-51078777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189924795	chr2:51078777-51078778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62140624	chr2:51078800-51078801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564685773	chr2:51078807-51078808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368510219	chr2:51078821-51078822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547149391	chr2:51078856-51078857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558116426	chr2:51078914-51078915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181364884	chr2:51078921-51078922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151254826	chr2:51078923-51078924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549142596	chr2:51078924-51078925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140442968	chr2:51078961-51078962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75793857	chr2:51079015-51079016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51070000-51078000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:51075000-51084400	Weak transcription	Ovary	ovary
3	chr2:51077200-51077800	Enhancers	Liver	Liver
4	chr2:51077200-51078200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:51077400-51078200	Weak transcription	Pancreas	Pancrea
6	chr2:51077400-51078400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:51077600-51078600	Enhancers	Fetal Brain Male	brain
8	chr2:51078000-51078200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:51078200-51078400	Enhancers	Fetal Brain Female	brain
10	chr2:51078200-51078800	Enhancers	Pancreas	Pancrea
11	chr2:51078200-51089600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:51078400-51079200	Weak transcription	Fetal Brain Female	brain
13	chr2:51078600-51079000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:51078600-51080200	Weak transcription	Fetal Brain Male	brain
15	chr2:51079200-51079400	Enhancers	Fetal Brain Female	brain
16	chr2:51079400-51080200	Weak transcription	Fetal Brain Female	brain
17	chr2:51080000-51080400	Enhancers	Brain Germinal Matrix	brain
18	chr2:51080200-51080600	Enhancers	Fetal Brain Male	brain
19	chr2:51080200-51080800	Enhancers	Fetal Brain Female	brain
20	chr2:51080400-51084400	Weak transcription	Brain Germinal Matrix	brain
21	chr2:51080600-51083200	Weak transcription	Fetal Brain Male	brain
22	chr2:51080800-51081200	Weak transcription	Fetal Brain Female	brain
23	chr2:51081200-51081800	Enhancers	Fetal Brain Female	brain
24	chr2:51081800-51082800	Weak transcription	Fetal Brain Female	brain
25	chr2:51082600-51085200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:51082800-51083200	Enhancers	Fetal Brain Female	brain
27	chr2:51083200-51084400	Enhancers	Fetal Brain Male	brain
28	chr2:51083200-51084800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:51083200-51108400	Weak transcription	Fetal Brain Female	brain
30	chr2:51083400-51084200	Enhancers	Fetal Kidney	kidney
31	chr2:51084400-51085000	Weak transcription	Fetal Brain Male	brain
32	chr2:51084400-51085200	Enhancers	Ovary	ovary
33	chr2:51084400-51086600	Enhancers	Brain Germinal Matrix	brain
34	chr2:51084800-51089600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:51085000-51085200	Enhancers	Fetal Brain Male	brain
36	chr2:51085200-51085600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:51085200-51085600	Enhancers	Brain Cingulate Gyrus	brain
38	chr2:51085200-51086000	Weak transcription	Ovary	ovary
39	chr2:51085200-51089600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:51085400-51085800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:51085600-51090200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr2:51085600-51090400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr2:51085800-51090000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:51086000-51086600	Enhancers	Ovary	ovary
45	chr2:51086200-51086600	Enhancers	Brain Angular Gyrus	brain
46	chr2:51086600-51089600	Weak transcription	Brain Germinal Matrix	brain
47	chr2:51086800-51087200	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr2:51089600-51089800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:51089600-51090400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:51089600-51091400	Enhancers	Pancreatic Islets	Pancreatic Islet

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