Variant report

Variant	nsv874049
Chromosome Location	chr2:50994255-51082754
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	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
2	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
3	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
4	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
5	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
6	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
7	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
8	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
9	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
10	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
11	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
12	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
13	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
14	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
16	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
17	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
18	CTCF	chr2:51013600-51013750	BE2_C	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
19	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
20	CTCF	chr2:51013640-51013790	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
21	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
22	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
23	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854
24	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
25	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
27	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
28	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
29	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
30	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
31	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
32	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
35	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
36	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
37	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
38	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
39	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:51013600-51013750	HEK293	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:51009760-51009910	HBMEC	blood vessel:	n/a	chr2:51009841-51009854
43	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
44	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
45	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
46	CTCF	chr2:51013660-51013810	GM12873	blood:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
47	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
48	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
49	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
50	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51001003-51001053	HMEC	breast:	n/a
2	chr2:51056884-51056934	SK-N-SH	brain:	n/a
3	chr2:51065673-51065723	BJ	skin:	n/a
4	chr2:51057548-51057598	NB4	blood:	n/a
5	chr2:51056884-51056934	GM12892	blood:	n/a
6	chr2:51074939-51074989	HRCEpiC	kidney:	n/a
7	chr2:51057218-51057268	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:51057548-51057598	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:51057548-51057598	HepG2	liver:	n/a
10	chr2:51074939-51074989	ovcar-3	ovarian:	n/a
11	chr2:51056822-51056872	SK-N-SH_RA	brain:	n/a
12	chr2:51057218-51057268	NH-A	brain:	n/a
13	chr2:51074939-51074989	HCM	heart:	n/a
14	chr2:51057548-51057598	Hela-S3	cervix:	n/a
15	chr2:51065673-51065723	GM06990	blood:	n/a
16	chr2:51001003-51001053	CMK	blood:	n/a
17	chr2:51074939-51074989	NT2-D1	testis:	n/a
18	chr2:51001003-51001053	LNCaP	prostate:	n/a
19	chr2:51056822-51056872	HepG2	liver:	n/a
20	chr2:51057548-51057598	NT2-D1	testis:	n/a
21	chr2:51065673-51065723	MCF10A-Er-Src	breast:	n/a
22	chr2:51074881-51074931	HEEpiC	esophagus:	n/a
23	chr2:51057218-51057268	AG10803	skin:	n/a
24	chr2:51065673-51065723	H1-hESC	embryonic stem cell:	embryo
25	chr2:51057218-51057268	BJ	skin:	n/a
26	chr2:51056822-51056872	HMEC	breast:	n/a
27	chr2:51056822-51056872	ovcar-3	ovarian:	n/a
28	chr2:51057548-51057598	SAEC	small airway:	n/a
29	chr2:51056884-51056934	A549	lung:	n/a
30	chr2:51065673-51065723	HCT-116	colon:	n/a
31	chr2:51074881-51074931	HCT-116	colon:	n/a
32	chr2:51074939-51074989	LNCaP	prostate:	n/a
33	chr2:51074881-51074931	HEK293	kidney:	embryo
34	chr2:51065673-51065723	HL-60	blood:	n/a
35	chr2:51001003-51001053	A549	lung:	n/a
36	chr2:51056884-51056934	PrEC	prostate:	n/a
37	chr2:51057218-51057268	AoSMC	blood vessel:	n/a
38	chr2:51074939-51074989	T-47D	breast:	n/a
39	chr2:51074881-51074931	BJ	skin:	n/a
40	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
41	chr2:51056884-51056934	HRE	kidney:	n/a
42	chr2:51057218-51057268	HCT-116	colon:	n/a
43	chr2:51056822-51056872	HRPEpiC	eye:	n/a
44	chr2:51057548-51057598	HMEC	breast:	n/a
45	chr2:51056884-51056934	SKMC	muscle:	n/a
46	chr2:51001003-51001053	AG09309	skin:	n/a
47	chr2:51074939-51074989	ECC-1	luminal epithelium:	n/a
48	chr2:51057548-51057598	AG09319	gingival:	n/a
49	chr2:51056884-51056934	NB4	blood:	n/a
50	chr2:51065673-51065723	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
2	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
3	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
4	chr2:51018306..51019906-chr2:51022210..51025087,2	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: 3204 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3204 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17502934	chr2:50994255-50994256	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540835823	chr2:50994272-50994273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547140922	chr2:50994293-50994294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560855667	chr2:50994295-50994296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573684073	chr2:50994341-50994342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537589514	chr2:50994343-50994344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141141326	chr2:50994346-50994347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375646351	chr2:50994381-50994382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575466215	chr2:50994403-50994404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546061541	chr2:50994416-50994417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184899494	chr2:50994435-50994436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369926665	chr2:50994449-50994450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537681068	chr2:50994551-50994552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529975457	chr2:50994602-50994603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540627772	chr2:50994618-50994619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374449029	chr2:50994652-50994653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189789769	chr2:50994653-50994654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529380836	chr2:50994701-50994702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549659245	chr2:50994713-50994714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557548901	chr2:50994748-50994749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181734820	chr2:50994805-50994806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562679736	chr2:50994916-50994917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570060100	chr2:50994945-50994946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533181519	chr2:50994954-50994955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551664800	chr2:50995019-50995020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62140593	chr2:50995057-50995058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76317829	chr2:50995117-50995118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548959280	chr2:50995138-50995139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567190805	chr2:50995160-50995161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559612531	chr2:50995203-50995204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553712435	chr2:50995254-50995255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116491322	chr2:50995268-50995269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146216853	chr2:50995283-50995284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575400671	chr2:50995288-50995289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539654793	chr2:50995304-50995305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374072878	chr2:50995360-50995361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186086192	chr2:50995367-50995368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540612657	chr2:50995437-50995438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562100879	chr2:50995442-50995443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573994398	chr2:50995500-50995501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535234341	chr2:50995503-50995504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189484366	chr2:50995512-50995513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137921227	chr2:50995549-50995550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529945856	chr2:50995589-50995590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111995079	chr2:50995605-50995606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76158812	chr2:50995607-50995608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10168800	chr2:50995619-50995620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181800032	chr2:50995653-50995654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10205006	chr2:50995664-50995665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186149645	chr2:50995665-50995666	Weak transcription Enhancers	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:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50983200-50996800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:50991800-50997000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:50992800-51000800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:50993000-50994400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:50993000-50998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:50993000-50999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:50993000-51000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr2:50993400-50995600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr2:50993400-50996000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr2:50993600-50996800	Weak transcription	Brain Anterior Caudate	brain
11	chr2:50994000-50996200	Weak transcription	Fetal Brain Female	brain
12	chr2:50994000-50996600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:50994200-50994800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:50994400-50995000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr2:50994800-50999800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr2:50995000-51000600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:50995600-50996200	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr2:50995800-50997400	Enhancers	Fetal Brain Male	brain
19	chr2:50996000-50996400	Enhancers	Brain Cingulate Gyrus	brain
20	chr2:50996000-50997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:50996000-50997400	Enhancers	Duodenum Mucosa	Duodenum
22	chr2:50996200-50996600	Enhancers	Fetal Intestine Small	intestine
23	chr2:50996200-50996600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr2:50996200-50996800	Enhancers	Fetal Brain Female	brain
25	chr2:50996400-50997200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:50996400-50997200	Enhancers	Fetal Intestine Large	intestine
27	chr2:50996400-51000800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr2:50996600-50997000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:50996600-50997000	Weak transcription	Fetal Intestine Small	intestine
30	chr2:50996600-50997400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:50996800-50997000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr2:50996800-50997000	Active TSS	Brain Anterior Caudate	brain
33	chr2:50997000-50997200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:50997000-50997200	Flanking Active TSS	Brain Anterior Caudate	brain
35	chr2:50997000-50997200	Enhancers	Fetal Intestine Small	intestine
36	chr2:50997000-50997200	Enhancers	Small Intestine	intestine
37	chr2:50997000-50997400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr2:50997000-50998800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:50997000-51001400	Enhancers	Liver	Liver
40	chr2:50997200-50998000	Weak transcription	Fetal Intestine Large	intestine
41	chr2:50997200-50998200	Weak transcription	Fetal Intestine Small	intestine
42	chr2:50997200-50999800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:50997200-51000800	Weak transcription	Brain Anterior Caudate	brain
44	chr2:50997200-51000800	Weak transcription	Brain Substantia Nigra	brain
45	chr2:50997400-50998000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr2:50997400-50999600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr2:50998000-51000800	Enhancers	Duodenum Mucosa	Duodenum
48	chr2:50998000-51001200	Enhancers	Fetal Intestine Large	intestine
49	chr2:50998200-51001000	Enhancers	Fetal Intestine Small	intestine
50	chr2:50998800-50999000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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