Variant report

Variant	nsv1005099
Chromosome Location	chr2:51002886-51136264
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	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
3	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
4	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
5	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
6	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
7	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
8	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
11	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
12	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
14	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
16	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
18	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
21	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
23	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
24	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
25	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
26	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
27	CTCF	chr2:51099689-51099932	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr2:51099780-51099930	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
30	CTCF	chr2:51086380-51086530	HCT-116	colon:	n/a	n/a
31	CTCF	chr2:51099809-51099906	Medullo	brain:	n/a	n/a
32	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
35	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
36	CTCF	chr2:51086400-51086492	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:51099740-51099890	RPTEC	kidney:	n/a	n/a
38	CTCF	chr2:51086380-51086530	Caco-2	colon:	n/a	n/a
39	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
40	CTCF	chr2:51099880-51100030	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:51099780-51099930	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr2:51099780-51099930	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:51099760-51099910	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr2:51099800-51099950	AG04450	lung:	n/a	n/a
46	CTCF	chr2:51099780-51099930	HEK293	kidney:	n/a	n/a
47	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
48	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
49	CTCF	chr2:51099850-51099874	Gliobla	brain:	n/a	n/a
50	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51057218-51057268	SK-N-SH	brain:	n/a
2	chr2:51074939-51074989	GM06990	blood:	n/a
3	chr2:51057218-51057268	SK-N-SH	brain:	n/a
4	chr2:51074939-51074989	GM06990	blood:	n/a
5	chr2:51056822-51056872	HL-60	blood:	n/a
6	chr2:51057218-51057268	GM12891	blood:	n/a
7	chr2:51074881-51074931	ProgFib	skin:	n/a
8	chr2:51057548-51057598	NT2-D1	testis:	n/a
9	chr2:51065673-51065723	HAEpiC	amniotic membrane:	n/a
10	chr2:51074881-51074931	AG04450	lung:	fetal
11	chr2:51074939-51074989	HRE	kidney:	n/a
12	chr2:51057218-51057268	NHBE	bronchial:	n/a
13	chr2:51056884-51056934	Jurkat	blood:	n/a
14	chr2:51057218-51057268	ovcar-3	ovarian:	n/a
15	chr2:51056822-51056872	NH-A	brain:	n/a
16	chr2:51056884-51056934	GM19239	blood:	n/a
17	chr2:51074939-51074989	HNPCEpiC	eye:	n/a
18	chr2:51074939-51074989	HUVEC	blood vessel:	n/a
19	chr2:51056822-51056872	Caco-2	colon:	n/a
20	chr2:51074939-51074989	HepG2	liver:	n/a
21	chr2:51074939-51074989	SK-N-SH	brain:	n/a
22	chr2:51056884-51056934	GM06990	blood:	n/a
23	chr2:51074881-51074931	MCF-7	breast:	n/a
24	chr2:51074939-51074989	BJ	skin:	n/a
25	chr2:51065673-51065723	NHDF-neo	bronchial:	n/a
26	chr2:51056884-51056934	LNCaP	prostate:	n/a
27	chr2:51074881-51074931	HCM	heart:	n/a
28	chr2:51057548-51057598	AG04449	skin:	fetal
29	chr2:51056884-51056934	GM12878	blood:	n/a
30	chr2:51074939-51074989	MCF10A-Er-Src	breast:	n/a
31	chr2:51056822-51056872	HNPCEpiC	eye:	n/a
32	chr2:51057548-51057598	PFSK-1	brain:	n/a
33	chr2:51057548-51057598	Jurkat	blood:	n/a
34	chr2:51074939-51074989	GM19239	blood:	n/a
35	chr2:51056884-51056934	Hepatocyte	liver:	n/a
36	chr2:51057218-51057268	NT2-D1	testis:	n/a
37	chr2:51057548-51057598	IMR90	lung:	fetal
38	chr2:51074939-51074989	PrEC	prostate:	n/a
39	chr2:51056822-51056872	RPTEC	kidney:	n/a
40	chr2:51057218-51057268	ProgFib	skin:	n/a
41	chr2:51056822-51056872	HEK293	kidney:	embryo
42	chr2:51057218-51057268	K562	blood:	n/a
43	chr2:51057218-51057268	HCF	heart:	n/a
44	chr2:51056822-51056872	NT2-D1	testis:	n/a
45	chr2:51057218-51057268	HCPEpiC	choroid plexus:	n/a
46	chr2:51074881-51074931	ovcar-3	ovarian:	n/a
47	chr2:51074881-51074931	HRE	kidney:	n/a
48	chr2:51065673-51065723	CMK	blood:	n/a
49	chr2:51065673-51065723	HL-60	blood:	n/a
50	chr2:51057218-51057268	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
2	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
3	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
4	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
5	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
6	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
7	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
8	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 4686 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4686 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60088848	chr2:51002910-51002911	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78493203	chr2:51002914-51002915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3850333	chr2:51002929-51002930	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs185619172	chr2:51002971-51002972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111888755	chr2:51003079-51003080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3902126	chr2:51003094-51003095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556646504	chr2:51003115-51003116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12465724	chr2:51003132-51003133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148563565	chr2:51003170-51003171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553669130	chr2:51003175-51003176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111419758	chr2:51003178-51003179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572227518	chr2:51003198-51003199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142907329	chr2:51003218-51003219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571109467	chr2:51003226-51003227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151116682	chr2:51003234-51003235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3902125	chr2:51003236-51003237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560859633	chr2:51003247-51003248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575586809	chr2:51003249-51003250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186782329	chr2:51003304-51003305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564581288	chr2:51003324-51003325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532095192	chr2:51003386-51003387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191997761	chr2:51003407-51003408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560450389	chr2:51003460-51003461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527899737	chr2:51003507-51003508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183914493	chr2:51003528-51003529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567961316	chr2:51003560-51003561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565919523	chr2:51003639-51003640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115830012	chr2:51003692-51003693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185400977	chr2:51003736-51003737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374349523	chr2:51003757-51003758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146965004	chr2:51003771-51003772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200157600	chr2:51003772-51003773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571648662	chr2:51003773-51003774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141384370	chr2:51003783-51003784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199761499	chr2:51003789-51003790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368896617	chr2:51003791-51003792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200773900	chr2:51003793-51003794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72221788	chr2:51003794-51003795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76405311	chr2:51003795-51003796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72172541	chr2:51003803-51003804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71880465	chr2:51003806-51003807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189982061	chr2:51003813-51003814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs70948727	chr2:51003816-51003817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554256345	chr2:51003817-51003818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527508764	chr2:51003825-51003826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182262429	chr2:51003852-51003853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536451323	chr2:51003888-51003889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554392362	chr2:51003920-51003921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536490038	chr2:51003984-51003985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575923265	chr2:51004016-51004017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51001200-51003400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr2:51001200-51004800	Weak transcription	Brain Anterior Caudate	brain
3	chr2:51001200-51004800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:51001200-51005600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:51001600-51004400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:51002400-51003000	Enhancers	Rectal Smooth Muscle	rectum
7	chr2:51002400-51003200	Enhancers	Duodenum Mucosa	Duodenum
8	chr2:51002600-51003000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:51002600-51003200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:51002600-51004600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:51002800-51003200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:51002800-51003200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:51002800-51005600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:51003000-51003200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr2:51003000-51003200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:51003000-51003200	Enhancers	Fetal Intestine Small	intestine
17	chr2:51003000-51004000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr2:51003200-51004400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr2:51003200-51004400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr2:51003400-51003600	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr2:51003600-51004800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:51004000-51005000	Enhancers	Rectal Smooth Muscle	rectum
23	chr2:51004400-51005000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:51004400-51005800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:51004400-51006000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr2:51004600-51005000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:51004800-51005000	Enhancers	Brain Cingulate Gyrus	brain
28	chr2:51004800-51005400	Enhancers	Brain Anterior Caudate	brain
29	chr2:51004800-51005400	Enhancers	Colon Smooth Muscle	Colon
30	chr2:51004800-51005600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:51005000-51005800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr2:51005000-51009800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr2:51005200-51005400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:51005400-51010400	Weak transcription	Colon Smooth Muscle	Colon
35	chr2:51005400-51013400	Weak transcription	Brain Anterior Caudate	brain
36	chr2:51005600-51005800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:51005600-51005800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:51006000-51008600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr2:51006400-51012800	Weak transcription	Fetal Brain Female	brain
40	chr2:51008000-51008200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr2:51008600-51009200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:51009200-51013400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:51009600-51010000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:51009800-51010000	Enhancers	Rectal Smooth Muscle	rectum
45	chr2:51010000-51010600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr2:51010400-51010800	Enhancers	Colon Smooth Muscle	Colon
47	chr2:51010800-51011000	Enhancers	Rectal Smooth Muscle	rectum
48	chr2:51010800-51013000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:51012600-51013800	Enhancers	Fetal Brain Male	brain
50	chr2:51012800-51014200	Enhancers	Fetal Brain Female	brain

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