Variant report

Variant	nsv933324
Chromosome Location	chr2:50998831-51099324
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	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
3	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
4	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
5	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
6	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
7	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
8	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
9	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
11	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
12	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
15	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
16	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
20	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
22	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
23	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
24	CTCF	chr2:51086380-51086530	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
26	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
27	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
28	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
29	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
30	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
31	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
32	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
33	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
35	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
37	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
38	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
39	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
40	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854
42	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
43	CTCF	chr2:51009760-51009910	HBMEC	blood vessel:	n/a	chr2:51009841-51009854
44	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
45	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
46	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
47	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
48	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
49	CTCF	chr2:51013600-51013750	BE2_C	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
50	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51056884-51056934	AG09319	gingival:	n/a
2	chr2:51056884-51056934	AG09319	gingival:	n/a
3	chr2:51056822-51056872	AG10803	skin:	n/a
4	chr2:51056822-51056872	LNCaP	prostate:	n/a
5	chr2:51056822-51056872	Hepatocyte	liver:	n/a
6	chr2:51001003-51001053	NHDF-neo	bronchial:	n/a
7	chr2:51056822-51056872	HEEpiC	esophagus:	n/a
8	chr2:51056884-51056934	NB4	blood:	n/a
9	chr2:51057548-51057598	HIPEpiC	eye:	n/a
10	chr2:51065673-51065723	HNPCEpiC	eye:	n/a
11	chr2:51001003-51001053	LNCaP	prostate:	n/a
12	chr2:51057548-51057598	NHDF-neo	bronchial:	n/a
13	chr2:51057548-51057598	PrEC	prostate:	n/a
14	chr2:51001003-51001053	GM06990	blood:	n/a
15	chr2:51001003-51001053	HMEC	breast:	n/a
16	chr2:51057218-51057268	MCF-7	breast:	n/a
17	chr2:51074881-51074931	MCF-7	breast:	n/a
18	chr2:51001003-51001053	GM12892	blood:	n/a
19	chr2:51057548-51057598	U87	brain:	n/a
20	chr2:51074881-51074931	Hela-S3	cervix:	n/a
21	chr2:51056822-51056872	HRCEpiC	kidney:	n/a
22	chr2:51065673-51065723	HRPEpiC	eye:	n/a
23	chr2:51074881-51074931	LNCaP	prostate:	n/a
24	chr2:51001003-51001053	Jurkat	blood:	n/a
25	chr2:51074881-51074931	GM12892	blood:	n/a
26	chr2:51074881-51074931	NHBE	bronchial:	n/a
27	chr2:51001003-51001053	A549	lung:	n/a
28	chr2:51065673-51065723	HepG2	liver:	n/a
29	chr2:51001003-51001053	BJ	skin:	n/a
30	chr2:51001003-51001053	HCPEpiC	choroid plexus:	n/a
31	chr2:51065673-51065723	H1-hESC	embryonic stem cell:	embryo
32	chr2:51074881-51074931	HEK293	kidney:	embryo
33	chr2:51056884-51056934	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:51057548-51057598	HUVEC	blood vessel:	n/a
35	chr2:51074881-51074931	HCF	heart:	n/a
36	chr2:51056884-51056934	Jurkat	blood:	n/a
37	chr2:51074939-51074989	ECC-1	luminal epithelium:	n/a
38	chr2:51065673-51065723	HEK293	kidney:	embryo
39	chr2:51001003-51001053	AG10803	skin:	n/a
40	chr2:51065673-51065723	BE2_C	brain:	n/a
41	chr2:51074939-51074989	GM12878	blood:	n/a
42	chr2:51057218-51057268	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:51056822-51056872	SKMC	muscle:	n/a
44	chr2:51056884-51056934	Hepatocyte	liver:	n/a
45	chr2:51057218-51057268	HCPEpiC	choroid plexus:	n/a
46	chr2:51001003-51001053	HCT-116	colon:	n/a
47	chr2:51056822-51056872	SAEC	small airway:	n/a
48	chr2:51074939-51074989	PrEC	prostate:	n/a
49	chr2:51074939-51074989	T-47D	breast:	n/a
50	chr2:51065673-51065723	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
2	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:51084150..51086897-chr2:51088805..51090362,2	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: 3659 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3659 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541818698	chr2:50998831-50998832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556728890	chr2:50998837-50998838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138306525	chr2:50998859-50998860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115668118	chr2:50998887-50998888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369318111	chr2:50998902-50998903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565457730	chr2:50998904-50998905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372790910	chr2:50998916-50998917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532777213	chr2:50998957-50998958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541331844	chr2:50998997-50998998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560007388	chr2:50999032-50999033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140244821	chr2:50999042-50999043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571031724	chr2:50999058-50999059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145191153	chr2:50999069-50999070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569754635	chr2:50999097-50999098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181528524	chr2:50999152-50999153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185690717	chr2:50999158-50999159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570282277	chr2:50999189-50999190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534833361	chr2:50999203-50999204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552951784	chr2:50999232-50999233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75737636	chr2:50999252-50999253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535423871	chr2:50999300-50999301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556981405	chr2:50999303-50999304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575341766	chr2:50999304-50999305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571702400	chr2:50999310-50999311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190594231	chr2:50999420-50999421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540752606	chr2:50999452-50999453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181054393	chr2:50999466-50999467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577329250	chr2:50999547-50999548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541619353	chr2:50999556-50999557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559741000	chr2:50999579-50999580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554227123	chr2:50999621-50999622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574305939	chr2:50999643-50999644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72889412	chr2:50999647-50999648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563317911	chr2:50999688-50999689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142497941	chr2:50999710-50999711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114122669	chr2:50999718-50999719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143077036	chr2:50999763-50999764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528226322	chr2:50999764-50999765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563602209	chr2:50999791-50999792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546764832	chr2:50999801-50999802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185889504	chr2:50999821-50999822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190134337	chr2:50999842-50999843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369811122	chr2:50999860-50999861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550917176	chr2:50999883-50999884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568837700	chr2:50999889-50999890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539452785	chr2:50999898-50999899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17562100	chr2:50999907-50999908	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs148254301	chr2:51000038-51000039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533687953	chr2:51000040-51000041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115865195	chr2:51000056-51000057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50992800-51000800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:50993000-50999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:50993000-51000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:50994800-50999800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:50995000-51000600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:50996400-51000800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:50997000-51001400	Enhancers	Liver	Liver
8	chr2:50997200-50999800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:50997200-51000800	Weak transcription	Brain Anterior Caudate	brain
10	chr2:50997200-51000800	Weak transcription	Brain Substantia Nigra	brain
11	chr2:50997400-50999600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:50998000-51000800	Enhancers	Duodenum Mucosa	Duodenum
13	chr2:50998000-51001200	Enhancers	Fetal Intestine Large	intestine
14	chr2:50998200-51001000	Enhancers	Fetal Intestine Small	intestine
15	chr2:50998800-50999000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:50998800-51001600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:50999000-51000000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:50999200-51000000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:50999200-51000000	Enhancers	Small Intestine	intestine
20	chr2:50999600-51001000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr2:50999800-51000000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:50999800-51001200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:51000000-51000400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:51000000-51001200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:51000400-51001000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:51000400-51001400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:51000600-51001000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:51000600-51001000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:51000600-51001200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:51000600-51001400	Enhancers	Fetal Kidney	kidney
31	chr2:51000600-51001600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:51000800-51001200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:51000800-51001200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr2:51000800-51001200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:51000800-51001200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:51000800-51001200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:51000800-51001200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:51000800-51001200	Enhancers	Brain Anterior Caudate	brain
39	chr2:51000800-51001200	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:51000800-51001200	Enhancers	Brain Substantia Nigra	brain
41	chr2:51000800-51001200	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr2:51000800-51001400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr2:51000800-51002400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr2:51001000-51001400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr2:51001000-51002600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:51001000-51002800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:51001200-51003400	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr2:51001200-51004800	Weak transcription	Brain Anterior Caudate	brain
49	chr2:51001200-51004800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr2:51001200-51005600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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