Variant report

Variant	nsv533300
Chromosome Location	chr2:50943480-51029090
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	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
6	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
7	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
12	CTCF	chr2:50973740-50973890	HFF	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
13	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
14	CTCF	chr2:50973642-50974009	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973760-50973910	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973625-50974108	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973780-50973930	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
19	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973721-50973966	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50973100-50973250	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973780-50973930	HMEC	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973780-50973930	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973760-50973910	AG04449	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
27	CTCF	chr2:50973760-50973910	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973740-50973890	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973773-50973916	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973520-50973670	HepG2	liver:	n/a	n/a
31	CTCF	chr2:50973752-50973932	GM12891	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:50973780-50973930	HBMEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973715-50973963	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
36	CTCF	chr2:51013600-51013750	HEK293	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
37	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
38	CTCF	chr2:50973740-50973890	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973717-50973974	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973741-50973938	GM19240	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
44	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973708-50973972	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973746-50973940	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973740-50973890	HBMEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973705-50973962	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50992829-50992879	BJ	skin:	n/a
2	chr2:50956659-50956709	NT2-D1	testis:	n/a
3	chr2:50992829-50992879	Caco-2	colon:	n/a
4	chr2:50956659-50956709	SK-N-SH	brain:	n/a
5	chr2:50992829-50992879	HL-60	blood:	n/a
6	chr2:50992829-50992879	HepG2	liver:	n/a
7	chr2:50992829-50992879	AoSMC	blood vessel:	n/a
8	chr2:51001003-51001053	GM06990	blood:	n/a
9	chr2:50992829-50992879	HIPEpiC	eye:	n/a
10	chr2:50992829-50992879	A549	lung:	n/a
11	chr2:50956659-50956709	H1-hESC	embryonic stem cell:	embryo
12	chr2:50956659-50956709	AG04450	lung:	fetal
13	chr2:51001003-51001053	GM12878	blood:	n/a
14	chr2:50956659-50956709	HMEC	breast:	n/a
15	chr2:50956659-50956709	RPTEC	kidney:	n/a
16	chr2:50956659-50956709	SKMC	muscle:	n/a
17	chr2:50956659-50956709	AG09319	gingival:	n/a
18	chr2:51001003-51001053	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:50956659-50956709	HepG2	liver:	n/a
20	chr2:50992829-50992879	HCM	heart:	n/a
21	chr2:51001003-51001053	MCF-7	breast:	n/a
22	chr2:51001003-51001053	HCT-116	colon:	n/a
23	chr2:50956659-50956709	GM06990	blood:	n/a
24	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
25	chr2:51001003-51001053	MCF10A-Er-Src	breast:	n/a
26	chr2:50956659-50956709	MCF-7	breast:	n/a
27	chr2:51001003-51001053	Caco-2	colon:	n/a
28	chr2:51001003-51001053	HCF	heart:	n/a
29	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
30	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
31	chr2:51001003-51001053	HepG2	liver:	n/a
32	chr2:50956659-50956709	GM12878	blood:	n/a
33	chr2:50956659-50956709	NH-A	brain:	n/a
34	chr2:50956659-50956709	HUVEC	blood vessel:	n/a
35	chr2:50992829-50992879	K562	blood:	n/a
36	chr2:50956659-50956709	NB4	blood:	n/a
37	chr2:50992829-50992879	SK-N-SH	brain:	n/a
38	chr2:50956659-50956709	HAEpiC	amniotic membrane:	n/a
39	chr2:50956659-50956709	GM12892	blood:	n/a
40	chr2:51001003-51001053	HCM	heart:	n/a
41	chr2:50992829-50992879	Jurkat	blood:	n/a
42	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
43	chr2:51001003-51001053	BJ	skin:	n/a
44	chr2:50992829-50992879	PFSK-1	brain:	n/a
45	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
46	chr2:50992829-50992879	T-47D	breast:	n/a
47	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
48	chr2:51001003-51001053	GM19239	blood:	n/a
49	chr2:50992829-50992879	HUVEC	blood vessel:	n/a
50	chr2:51001003-51001053	AG09319	gingival:	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	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
6	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
9	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
10	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:

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

Extended variants
information (count: 2910 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2910 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529744628	chr2:50943491-50943492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1518553	chr2:50943528-50943529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192741278	chr2:50943570-50943571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556288810	chr2:50943612-50943613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577577132	chr2:50943639-50943640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545312973	chr2:50943650-50943651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560384026	chr2:50943658-50943659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113876315	chr2:50943662-50943663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572331323	chr2:50943741-50943742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542834754	chr2:50943768-50943769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535569403	chr2:50943771-50943772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534137693	chr2:50943783-50943784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531303455	chr2:50943796-50943797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144502981	chr2:50943802-50943803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148421761	chr2:50943820-50943821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184043940	chr2:50943849-50943850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547743728	chr2:50943874-50943875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565966143	chr2:50943884-50943885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529940650	chr2:50943940-50943941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548080321	chr2:50943987-50943988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188578823	chr2:50943992-50943993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569787985	chr2:50944008-50944009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537965134	chr2:50944009-50944010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556588680	chr2:50944081-50944082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571331176	chr2:50944119-50944120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538624173	chr2:50944189-50944190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144098862	chr2:50944190-50944191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181701551	chr2:50944261-50944262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543250194	chr2:50944264-50944265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554867555	chr2:50944265-50944266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576540081	chr2:50944278-50944279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543167709	chr2:50944290-50944291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564944365	chr2:50944315-50944316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532179955	chr2:50944334-50944335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541018876	chr2:50944354-50944355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186053384	chr2:50944416-50944417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537462122	chr2:50944432-50944433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs17040973	chr2:50944481-50944482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189632316	chr2:50944483-50944484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182207891	chr2:50944659-50944660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549888661	chr2:50944673-50944674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571390411	chr2:50944780-50944781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538684520	chr2:50944862-50944863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553744964	chr2:50944868-50944869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565690543	chr2:50944870-50944871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536553884	chr2:50944909-50944910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200691473	chr2:50944944-50944945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376902980	chr2:50944957-50944958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs80339104	chr2:50945062-50945063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185990677	chr2:50945107-50945108	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:452 , 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	chr2:50940600-50944800	Weak transcription	Liver	Liver
5	chr2:50941600-50945600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:50942000-50947000	Weak transcription	Fetal Kidney	kidney
7	chr2:50942000-50947600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr2:50943200-50944400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:50944400-50946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:50944800-50945400	Enhancers	Liver	Liver
11	chr2:50945400-50945600	Enhancers	Brain Substantia Nigra	brain
12	chr2:50945400-50945800	Enhancers	Brain Hippocampus Middle	brain
13	chr2:50945400-50946600	Weak transcription	Liver	Liver
14	chr2:50945600-50946000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:50945600-50947400	Weak transcription	Brain Substantia Nigra	brain
16	chr2:50945800-50946000	Enhancers	Brain Anterior Caudate	brain
17	chr2:50945800-50947600	Weak transcription	Brain Hippocampus Middle	brain
18	chr2:50946000-50947200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:50946000-50948000	Weak transcription	Brain Anterior Caudate	brain
20	chr2:50946600-50948600	Enhancers	Liver	Liver
21	chr2:50946800-50947200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr2:50947000-50947600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr2:50947000-50947600	Enhancers	Fetal Kidney	kidney
24	chr2:50947000-50948400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:50947000-50948800	Enhancers	Brain Angular Gyrus	brain
26	chr2:50947200-50947600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr2:50947200-50947800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:50947200-50948400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:50947200-50948600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:50947200-50948600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:50947400-50947600	Enhancers	Fetal Brain Male	brain
32	chr2:50947400-50947800	Enhancers	Brain Substantia Nigra	brain
33	chr2:50947400-50948200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:50947400-50948400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr2:50947400-50948600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr2:50947400-50948600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:50947400-50948600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:50947400-50948600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:50947400-50948800	Enhancers	Brain Germinal Matrix	brain
40	chr2:50947600-50948000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr2:50947600-50948200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:50947600-50948200	Weak transcription	Fetal Brain Male	brain
43	chr2:50947600-50948600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr2:50947600-50948800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr2:50947600-50948800	Enhancers	Brain Hippocampus Middle	brain
46	chr2:50947600-50948800	Enhancers	Fetal Brain Female	brain
47	chr2:50947600-50950800	Weak transcription	Fetal Kidney	kidney
48	chr2:50947800-50948000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr2:50947800-50948400	Enhancers	Fetal Muscle Leg	muscle
50	chr2:50947800-50948600	Enhancers	Brain Cingulate Gyrus	brain

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