Variant report

Variant	nsv457585
Chromosome Location	chr2:50963542-51039129
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	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
2	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
3	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
4	CTCF	chr2:50973732-50973965	GM19238	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
5	CTCF	chr2:50973732-50973938	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
6	CTCF	chr2:50973740-50973890	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
7	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
8	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
9	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
10	CTCF	chr2:50973773-50973916	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
11	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
12	CTCF	chr2:50973751-50973938	GM12892	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
13	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973740-50973890	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973740-50973890	SAEC	small airway:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973780-50973930	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973780-50973930	HRE	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973820-50973970	GM12868	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973740-50973890	GM12873	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
22	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
23	CTCF	chr2:50973720-50973870	HVMF	connective:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973740-50973931	GM10266	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973760-50973910	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973756-50973917	GM20000	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973800-50973950	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
30	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973720-50973870	GM12868	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973780-50973930	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
35	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
36	CTCF	chr2:50973641-50974055	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973715-50973963	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973740-50973890	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973728-50973980	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973705-50973962	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973708-50973972	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
44	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973780-50973930	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50978545-50978604	Medullo	brain:	n/a	n/a
48	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
49	CTCF	chr2:50973740-50973890	HBMEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973720-50973870	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
2	chr2:51001003-51001053	SAEC	small airway:	n/a
3	chr2:51001003-51001053	HIPEpiC	eye:	n/a
4	chr2:51001003-51001053	SK-N-MC	brain:	n/a
5	chr2:51001003-51001053	HRE	kidney:	n/a
6	chr2:51001003-51001053	NB4	blood:	n/a
7	chr2:50992829-50992879	HCPEpiC	choroid plexus:	n/a
8	chr2:51001003-51001053	K562	blood:	n/a
9	chr2:51001003-51001053	GM06990	blood:	n/a
10	chr2:50992829-50992879	NHBE	bronchial:	n/a
11	chr2:51001003-51001053	MCF-7	breast:	n/a
12	chr2:50992829-50992879	LNCaP	prostate:	n/a
13	chr2:50992829-50992879	AG09309	skin:	n/a
14	chr2:50992829-50992879	HRE	kidney:	n/a
15	chr2:51001003-51001053	GM19239	blood:	n/a
16	chr2:50992829-50992879	K562	blood:	n/a
17	chr2:51001003-51001053	MCF10A-Er-Src	breast:	n/a
18	chr2:51001003-51001053	IMR90	lung:	fetal
19	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
20	chr2:51001003-51001053	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:50992829-50992879	Hepatocyte	liver:	n/a
22	chr2:51001003-51001053	AG04450	lung:	fetal
23	chr2:51001003-51001053	HCPEpiC	choroid plexus:	n/a
24	chr2:50992829-50992879	CMK	blood:	n/a
25	chr2:51001003-51001053	SK-N-SH_RA	brain:	n/a
26	chr2:50992829-50992879	PrEC	prostate:	n/a
27	chr2:50992829-50992879	HAEpiC	amniotic membrane:	n/a
28	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
29	chr2:50992829-50992879	HEEpiC	esophagus:	n/a
30	chr2:51001003-51001053	H1-hESC	embryonic stem cell:	embryo
31	chr2:50992829-50992879	MCF-7	breast:	n/a
32	chr2:50992829-50992879	SK-N-SH	brain:	n/a
33	chr2:50992829-50992879	Hela-S3	cervix:	n/a
34	chr2:51001003-51001053	SKMC	muscle:	n/a
35	chr2:51001003-51001053	PrEC	prostate:	n/a
36	chr2:50992829-50992879	NB4	blood:	n/a
37	chr2:50992829-50992879	HCF	heart:	n/a
38	chr2:51001003-51001053	PANC-1	pancreas:	n/a
39	chr2:51001003-51001053	AG09309	skin:	n/a
40	chr2:51001003-51001053	HCT-116	colon:	n/a
41	chr2:50992829-50992879	ECC-1	luminal epithelium:	n/a
42	chr2:51001003-51001053	HL-60	blood:	n/a
43	chr2:51001003-51001053	HCM	heart:	n/a
44	chr2:51001003-51001053	ProgFib	skin:	n/a
45	chr2:51001003-51001053	T-47D	breast:	n/a
46	chr2:50992829-50992879	A549	lung:	n/a
47	chr2:50992829-50992879	AG10803	skin:	n/a
48	chr2:50992829-50992879	ovcar-3	ovarian:	n/a
49	chr2:51001003-51001053	PFSK-1	brain:	n/a
50	chr2:50992829-50992879	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
2	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
3	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
6	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
7	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:

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

Extended variants
information (count: 2527 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2527 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144557641	chr2:50965442-50965443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs13006909	chr2:50965462-50965463	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs146629558	chr2:50965465-50965466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10174285	chr2:50965496-50965497	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528066139	chr2:50965515-50965516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191464702	chr2:50965519-50965520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568019280	chr2:50965569-50965570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535703026	chr2:50965580-50965581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4971693	chr2:50965589-50965590	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551053262	chr2:50965592-50965593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1646427	chr2:50965616-50965617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs367560457	chr2:50965624-50965625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72887593	chr2:50965634-50965635	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs117270703	chr2:50965659-50965660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148833501	chr2:50965726-50965727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201336451	chr2:50965766-50965767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553360838	chr2:50965769-50965770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575225248	chr2:50965835-50965836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117483849	chr2:50966025-50966026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115683868	chr2:50966069-50966070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531117615	chr2:50966089-50966090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545620581	chr2:50966127-50966128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563833954	chr2:50966140-50966141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9677055	chr2:50966158-50966159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1713859	chr2:50966161-50966162	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546199165	chr2:50966172-50966173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150957963	chr2:50966173-50966174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529197022	chr2:50966204-50966205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183577292	chr2:50966205-50966206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140755241	chr2:50966219-50966220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539613043	chr2:50966223-50966224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559142791	chr2:50966253-50966254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570963095	chr2:50966257-50966258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1546667	chr2:50966283-50966284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs9677069	chr2:50966288-50966289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188912756	chr2:50966293-50966294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574751335	chr2:50966343-50966344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535803917	chr2:50966353-50966354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145861836	chr2:50966354-50966355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575793833	chr2:50966368-50966369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372318154	chr2:50966380-50966381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376238163	chr2:50966408-50966409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9678417	chr2:50966411-50966412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9678418	chr2:50966422-50966423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368938721	chr2:50966439-50966440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9677804	chr2:50966550-50966551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545990000	chr2:50966564-50966565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562510400	chr2:50966643-50966644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375472942	chr2:50966684-50966685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531332978	chr2:50966705-50966706	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
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
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50965400-50966200	Enhancers	Brain Germinal Matrix	brain
2	chr2:50966200-50967800	Weak transcription	Brain Germinal Matrix	brain
3	chr2:50967800-50968400	Enhancers	Brain Germinal Matrix	brain
4	chr2:50971800-50972200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:50972200-50975800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:50972200-50978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:50974200-50974400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:50974200-50974400	Weak transcription	Brain Germinal Matrix	brain
9	chr2:50974400-50974600	Enhancers	Brain Hippocampus Middle	brain
10	chr2:50974400-50975200	Enhancers	HSMMtube	muscle
11	chr2:50974400-50976200	Enhancers	Brain Germinal Matrix	brain
12	chr2:50974400-50978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:50975000-50976000	Enhancers	Fetal Muscle Leg	muscle
14	chr2:50975000-50976800	Enhancers	Fetal Brain Female	brain
15	chr2:50975200-50975800	Enhancers	Fetal Brain Male	brain
16	chr2:50975200-50977200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:50975400-50975600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:50975400-50975800	Enhancers	Brain Hippocampus Middle	brain
19	chr2:50975600-50975800	Enhancers	Fetal Stomach	stomach
20	chr2:50975600-50975800	Enhancers	Psoas Muscle	Psoas
21	chr2:50975600-50976200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
22	chr2:50975800-50976200	Active TSS	Brain Anterior Caudate	brain
23	chr2:50975800-50976200	Active TSS	Brain Hippocampus Middle	brain
24	chr2:50975800-50976200	Active TSS	Brain Substantia Nigra	brain
25	chr2:50975800-50976200	Enhancers	Fetal Kidney	kidney
26	chr2:50975800-50976600	Weak transcription	Fetal Stomach	stomach
27	chr2:50975800-50977000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:50975800-50978400	Weak transcription	Fetal Brain Male	brain
29	chr2:50976000-50977200	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:50976000-50978000	Weak transcription	Psoas Muscle	Psoas
31	chr2:50976000-50978600	Weak transcription	Fetal Muscle Leg	muscle
32	chr2:50976200-50976600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr2:50976200-50976800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:50976200-50977400	Enhancers	Brain Hippocampus Middle	brain
35	chr2:50976200-50978200	Weak transcription	Brain Germinal Matrix	brain
36	chr2:50976200-50982800	Weak transcription	Brain Substantia Nigra	brain
37	chr2:50976400-50976600	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr2:50976600-50979800	Enhancers	Fetal Stomach	stomach
39	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:50976800-50977400	Weak transcription	Fetal Brain Female	brain
41	chr2:50976800-50978200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:50976800-50978200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr2:50977000-50982200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:50977200-50978400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr2:50977400-50983600	Weak transcription	Brain Hippocampus Middle	brain
46	chr2:50977400-50984400	Enhancers	Fetal Brain Female	brain
47	chr2:50978200-50978800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:50978200-50979200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:50978200-50979200	Enhancers	Colon Smooth Muscle	Colon
50	chr2:50978200-50979400	Enhancers	Duodenum Smooth Muscle	Duodenum

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