Variant report

Variant	nsv1000302
Chromosome Location	chr2:50977979-51086349
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	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
4	CEBPB	chr2:51077746-51078099	IMR90	lung:	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	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
8	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
10	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
11	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
12	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
14	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
15	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
16	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
17	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
18	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
19	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
20	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
22	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
23	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
24	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
25	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
26	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
27	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
28	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
29	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
31	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
32	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
35	CTCF	chr2:51013660-51013810	GM12873	blood:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
36	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
37	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
38	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854
39	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:50978500-50978650	HMEC	breast:	n/a	n/a
42	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
43	CTCF	chr2:51013640-51013790	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
44	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
45	CTCF	chr2:51013600-51013750	BE2_C	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
46	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
47	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
48	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
50	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51065673-51065723	NT2-D1	testis:	n/a
2	chr2:51056822-51056872	PFSK-1	brain:	n/a
3	chr2:51074881-51074931	HEK293	kidney:	embryo
4	chr2:50992829-50992879	Caco-2	colon:	n/a
5	chr2:51001003-51001053	RPTEC	kidney:	n/a
6	chr2:51057548-51057598	T-47D	breast:	n/a
7	chr2:51056822-51056872	NT2-D1	testis:	n/a
8	chr2:51001003-51001053	NH-A	brain:	n/a
9	chr2:51074881-51074931	CMK	blood:	n/a
10	chr2:51074939-51074989	K562	blood:	n/a
11	chr2:51001003-51001053	SAEC	small airway:	n/a
12	chr2:51074939-51074989	HepG2	liver:	n/a
13	chr2:51056822-51056872	GM06990	blood:	n/a
14	chr2:51057548-51057598	Hepatocyte	liver:	n/a
15	chr2:51056884-51056934	GM12892	blood:	n/a
16	chr2:51056884-51056934	HL-60	blood:	n/a
17	chr2:51057548-51057598	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:51056822-51056872	SAEC	small airway:	n/a
19	chr2:50992829-50992879	T-47D	breast:	n/a
20	chr2:50992829-50992879	HRPEpiC	eye:	n/a
21	chr2:51065673-51065723	LNCaP	prostate:	n/a
22	chr2:51057218-51057268	HEK293	kidney:	embryo
23	chr2:51056884-51056934	PrEC	prostate:	n/a
24	chr2:51001003-51001053	Caco-2	colon:	n/a
25	chr2:51057548-51057598	ovcar-3	ovarian:	n/a
26	chr2:50992829-50992879	HL-60	blood:	n/a
27	chr2:51001003-51001053	PrEC	prostate:	n/a
28	chr2:50992829-50992879	H1-hESC	embryonic stem cell:	embryo
29	chr2:51056884-51056934	Hela-S3	cervix:	n/a
30	chr2:51065673-51065723	A549	lung:	n/a
31	chr2:51056884-51056934	RPTEC	kidney:	n/a
32	chr2:51074881-51074931	NH-A	brain:	n/a
33	chr2:51056822-51056872	SKMC	muscle:	n/a
34	chr2:51056884-51056934	AoSMC	blood vessel:	n/a
35	chr2:51056884-51056934	HMEC	breast:	n/a
36	chr2:51056822-51056872	GM12892	blood:	n/a
37	chr2:51057218-51057268	A549	lung:	n/a
38	chr2:51074881-51074931	NHBE	bronchial:	n/a
39	chr2:51057218-51057268	HUVEC	blood vessel:	n/a
40	chr2:50992829-50992879	SKMC	muscle:	n/a
41	chr2:51001003-51001053	HAEpiC	amniotic membrane:	n/a
42	chr2:51074881-51074931	AG04450	lung:	fetal
43	chr2:51074939-51074989	AG10803	skin:	n/a
44	chr2:50992829-50992879	BE2_C	brain:	n/a
45	chr2:51056884-51056934	HepG2	liver:	n/a
46	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
47	chr2:51074881-51074931	Hela-S3	cervix:	n/a
48	chr2:51056884-51056934	MCF10A-Er-Src	breast:	n/a
49	chr2:51074939-51074989	NT2-D1	testis:	n/a
50	chr2:51057548-51057598	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
2	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
5	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
6	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
7	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
8	chr2:50985182..50988156-chr2:50995412..50998213,2	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: 3940 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3940 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9752357	chr2:50977979-50977980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9752358	chr2:50977990-50977991	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs529717670	chr2:50977998-50977999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547800698	chr2:50978055-50978056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556653855	chr2:50978108-50978109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372372718	chr2:50978152-50978153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576835882	chr2:50978194-50978195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530745431	chr2:50978221-50978222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74814705	chr2:50978242-50978243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570600340	chr2:50978249-50978250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186069785	chr2:50978259-50978260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546436310	chr2:50978282-50978283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545985465	chr2:50978307-50978308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189490861	chr2:50978371-50978372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566179013	chr2:50978393-50978394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60477852	chr2:50978429-50978430	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149399630	chr2:50978466-50978467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181807696	chr2:50978527-50978528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552854054	chr2:50978549-50978550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537782970	chr2:50978571-50978572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375708021	chr2:50978576-50978577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559201193	chr2:50978579-50978580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572986835	chr2:50978604-50978605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11893978	chr2:50978621-50978622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11894041	chr2:50978637-50978638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17502643	chr2:50978651-50978652	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371343983	chr2:50978663-50978664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186025835	chr2:50978684-50978685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548510347	chr2:50978739-50978740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190929954	chr2:50978740-50978741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562982479	chr2:50978752-50978753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182491723	chr2:50978768-50978769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186709439	chr2:50978786-50978787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190071355	chr2:50978800-50978801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528108953	chr2:50978805-50978806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144847781	chr2:50978837-50978838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568085229	chr2:50978863-50978864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561946136	chr2:50978873-50978874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530942031	chr2:50978944-50978945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548809308	chr2:50978956-50978957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570314908	chr2:50978969-50978970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368861820	chr2:50979008-50979009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537735997	chr2:50979027-50979028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140159354	chr2:50979078-50979079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570807732	chr2:50979148-50979149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183054538	chr2:50979207-50979208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553400716	chr2:50979254-50979255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574605096	chr2:50979314-50979315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374532984	chr2:50979315-50979316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187230257	chr2:50979355-50979356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	21990379	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:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50972200-50978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:50974400-50978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:50975800-50978400	Weak transcription	Fetal Brain Male	brain
4	chr2:50976000-50978000	Weak transcription	Psoas Muscle	Psoas
5	chr2:50976000-50978600	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:50976200-50978200	Weak transcription	Brain Germinal Matrix	brain
7	chr2:50976200-50982800	Weak transcription	Brain Substantia Nigra	brain
8	chr2:50976600-50979800	Enhancers	Fetal Stomach	stomach
9	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr2:50976800-50978200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:50976800-50978200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr2:50977000-50982200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:50977200-50978400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr2:50977400-50983600	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:50977400-50984400	Enhancers	Fetal Brain Female	brain
16	chr2:50978200-50978800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:50978200-50979200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:50978200-50979200	Enhancers	Colon Smooth Muscle	Colon
19	chr2:50978200-50979400	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr2:50978200-50979600	Enhancers	Rectal Smooth Muscle	rectum
21	chr2:50978200-50980400	Enhancers	Brain Germinal Matrix	brain
22	chr2:50978200-50980400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr2:50978400-50978800	Enhancers	NH-A	brain
24	chr2:50978400-50980800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:50978400-50984400	Enhancers	Fetal Brain Male	brain
26	chr2:50978600-50978800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:50978600-50979200	Enhancers	Fetal Muscle Leg	muscle
28	chr2:50978800-50979400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:50979200-50982200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:50979200-50982200	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:50979400-50979600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr2:50979400-50980800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:50979600-50982400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:50980200-50981000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:50980400-50980800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:50980400-50981200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr2:50980400-50981800	Weak transcription	Brain Germinal Matrix	brain
38	chr2:50980800-50982000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:50980800-50984000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:50981200-50983400	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr2:50981800-50982600	Enhancers	Brain Germinal Matrix	brain
42	chr2:50982000-50983200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr2:50982200-50982400	Enhancers	Fetal Muscle Leg	muscle
44	chr2:50982200-50982600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:50982200-50982600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:50982400-50982600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr2:50982600-50983400	Weak transcription	Brain Germinal Matrix	brain
48	chr2:50982600-50991200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:50982800-50983000	Enhancers	Brain Substantia Nigra	brain
50	chr2:50983000-50983200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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