Variant report

Variant	nsv998921
Chromosome Location	chr2:50945471-51040820
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	chr2:50955596-50955702	K562	blood:	n/a	n/a
2	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
4	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
8	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
11	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
13	CTCF	chr2:50973740-50973890	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50978545-50978604	Medullo	brain:	n/a	n/a
16	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
17	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973760-50973910	HMF	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973740-50973890	NB4	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973820-50973970	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50973708-50973972	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973722-50973924	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973773-50973916	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973760-50973910	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973800-50973950	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
30	CTCF	chr2:50973747-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50969658-50969686	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
34	CTCF	chr2:50973740-50973890	GM12867	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973728-50973980	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973820-50973970	GM12868	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
38	CTCF	chr2:50973720-50973870	AoAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973743-50973945	Pancreas_OC	pancreas:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
44	CTCF	chr2:50973700-50973850	NHDF-neo	bronchial:	n/a	chr2:50973841-50973849
45	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
46	CTCF	chr2:50973741-50973938	GM19240	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973740-50973890	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973740-50973890	HFF	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973729-50973949	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973760-50973910	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	AG04450	lung:	fetal
2	chr2:50956659-50956709	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:50992829-50992879	SK-N-SH_RA	brain:	n/a
4	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
5	chr2:50992829-50992879	HCPEpiC	choroid plexus:	n/a
6	chr2:51001003-51001053	HCM	heart:	n/a
7	chr2:50992829-50992879	Caco-2	colon:	n/a
8	chr2:50956659-50956709	BE2_C	brain:	n/a
9	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
10	chr2:51001003-51001053	H1-hESC	embryonic stem cell:	embryo
11	chr2:51001003-51001053	ProgFib	skin:	n/a
12	chr2:50992829-50992879	PFSK-1	brain:	n/a
13	chr2:50956659-50956709	HMEC	breast:	n/a
14	chr2:50992829-50992879	AG10803	skin:	n/a
15	chr2:50992829-50992879	U87	brain:	n/a
16	chr2:50992829-50992879	SKMC	muscle:	n/a
17	chr2:51001003-51001053	AG04449	skin:	fetal
18	chr2:50992829-50992879	HCT-116	colon:	n/a
19	chr2:50992829-50992879	NHDF-neo	bronchial:	n/a
20	chr2:50956659-50956709	HRPEpiC	eye:	n/a
21	chr2:50956659-50956709	PANC-1	pancreas:	n/a
22	chr2:51001003-51001053	MCF10A-Er-Src	breast:	n/a
23	chr2:50992829-50992879	SK-N-MC	brain:	n/a
24	chr2:51001003-51001053	BJ	skin:	n/a
25	chr2:51001003-51001053	SK-N-SH	brain:	n/a
26	chr2:51001003-51001053	MCF-7	breast:	n/a
27	chr2:50992829-50992879	GM12892	blood:	n/a
28	chr2:51001003-51001053	AG04450	lung:	fetal
29	chr2:50956659-50956709	NH-A	brain:	n/a
30	chr2:50992829-50992879	HRPEpiC	eye:	n/a
31	chr2:50992829-50992879	Jurkat	blood:	n/a
32	chr2:51001003-51001053	IMR90	lung:	fetal
33	chr2:51001003-51001053	HCT-116	colon:	n/a
34	chr2:50956659-50956709	GM12892	blood:	n/a
35	chr2:51001003-51001053	GM06990	blood:	n/a
36	chr2:50992829-50992879	Hepatocyte	liver:	n/a
37	chr2:50992829-50992879	CMK	blood:	n/a
38	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
39	chr2:50992829-50992879	AG04450	lung:	fetal
40	chr2:50956659-50956709	HL-60	blood:	n/a
41	chr2:50956659-50956709	HRE	kidney:	n/a
42	chr2:50956659-50956709	GM06990	blood:	n/a
43	chr2:50956659-50956709	HIPEpiC	eye:	n/a
44	chr2:50956659-50956709	ECC-1	luminal epithelium:	n/a
45	chr2:51001003-51001053	NH-A	brain:	n/a
46	chr2:50992829-50992879	A549	lung:	n/a
47	chr2:50992829-50992879	RPTEC	kidney:	n/a
48	chr2:50992829-50992879	NHBE	bronchial:	n/a
49	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
50	chr2:50956659-50956709	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
6	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
7	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
8	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
9	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
10	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: 3148 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3148 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4971565	chr2:50945471-50945472	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs13396432	chr2:50945519-50945520	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548628842	chr2:50945524-50945525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558470442	chr2:50945633-50945634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376325748	chr2:50945660-50945661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs858940	chr2:50945699-50945700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559198582	chr2:50945703-50945704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10490220	chr2:50945777-50945778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs552774391	chr2:50945807-50945808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553077379	chr2:50945815-50945816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574379719	chr2:50945838-50945839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568465452	chr2:50945876-50945877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114178387	chr2:50945892-50945893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs858941	chr2:50945902-50945903	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545643742	chr2:50945929-50945930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563948613	chr2:50945991-50945992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528237314	chr2:50945996-50945997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547505476	chr2:50946027-50946028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59462573	chr2:50946072-50946073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139912641	chr2:50946078-50946079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185611915	chr2:50946099-50946100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144755781	chr2:50946105-50946106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530081595	chr2:50946159-50946160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548561526	chr2:50946168-50946169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541968464	chr2:50946220-50946221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569904387	chr2:50946277-50946278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190073049	chr2:50946278-50946279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183059203	chr2:50946290-50946291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17040976	chr2:50946373-50946374	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs576413339	chr2:50946458-50946459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535211002	chr2:50946460-50946461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187218966	chr2:50946514-50946515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574462701	chr2:50946530-50946531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535150259	chr2:50946535-50946536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556916097	chr2:50946539-50946540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574850096	chr2:50946580-50946581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545707167	chr2:50946581-50946582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577561197	chr2:50946630-50946631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564010738	chr2:50946665-50946666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112113177	chr2:50946676-50946677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193111141	chr2:50946724-50946725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375244039	chr2:50946771-50946772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546402986	chr2:50946786-50946787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143529042	chr2:50946791-50946792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183927528	chr2:50946792-50946793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546109753	chr2:50946824-50946825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201052080	chr2:50946825-50946826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555810116	chr2:50946830-50946831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541918147	chr2:50946831-50946832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373306297	chr2:50946839-50946840	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
Acute myeloid leukemia	20729466	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:50935000-50947400	Weak transcription	Fetal Brain Male	brain
3	chr2:50939800-50947600	Weak transcription	Fetal Brain Female	brain
4	chr2:50941600-50945600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:50942000-50947000	Weak transcription	Fetal Kidney	kidney
6	chr2:50942000-50947600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:50944400-50946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:50945400-50945600	Enhancers	Brain Substantia Nigra	brain
9	chr2:50945400-50945800	Enhancers	Brain Hippocampus Middle	brain
10	chr2:50945400-50946600	Weak transcription	Liver	Liver
11	chr2:50945600-50946000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:50945600-50947400	Weak transcription	Brain Substantia Nigra	brain
13	chr2:50945800-50946000	Enhancers	Brain Anterior Caudate	brain
14	chr2:50945800-50947600	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:50946000-50947200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:50946000-50948000	Weak transcription	Brain Anterior Caudate	brain
17	chr2:50946600-50948600	Enhancers	Liver	Liver
18	chr2:50946800-50947200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr2:50947000-50947600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:50947000-50947600	Enhancers	Fetal Kidney	kidney
21	chr2:50947000-50948400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:50947000-50948800	Enhancers	Brain Angular Gyrus	brain
23	chr2:50947200-50947600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr2:50947200-50947800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:50947200-50948400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:50947200-50948600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:50947200-50948600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:50947400-50947600	Enhancers	Fetal Brain Male	brain
29	chr2:50947400-50947800	Enhancers	Brain Substantia Nigra	brain
30	chr2:50947400-50948200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:50947400-50948400	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr2:50947400-50948600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:50947400-50948600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:50947400-50948600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr2:50947400-50948600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:50947400-50948800	Enhancers	Brain Germinal Matrix	brain
37	chr2:50947600-50948000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr2:50947600-50948200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr2:50947600-50948200	Weak transcription	Fetal Brain Male	brain
40	chr2:50947600-50948600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr2:50947600-50948800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr2:50947600-50948800	Enhancers	Brain Hippocampus Middle	brain
43	chr2:50947600-50948800	Enhancers	Fetal Brain Female	brain
44	chr2:50947600-50950800	Weak transcription	Fetal Kidney	kidney
45	chr2:50947800-50948000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr2:50947800-50948400	Enhancers	Fetal Muscle Leg	muscle
47	chr2:50947800-50948600	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:50947800-50948600	Enhancers	Fetal Stomach	stomach
49	chr2:50947800-50949800	Weak transcription	Brain Substantia Nigra	brain
50	chr2:50948000-50948200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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