Variant report

Variant	nsv1015006
Chromosome Location	chr2:50923733-50996952
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	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
8	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
9	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr2:50973820-50973970	HVMF	connective:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
11	CTCF	chr2:50973733-50973956	GM13977	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
12	CTCF	chr2:50973740-50973890	HRE	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
13	CTCF	chr2:50973740-50973890	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973715-50973963	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973705-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973740-50973890	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973760-50973910	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50978545-50978604	Medullo	brain:	n/a	n/a
21	CTCF	chr2:50973572-50973669	Gliobla	brain:	n/a	n/a
22	CTCF	chr2:50973780-50973930	HBMEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973685-50974004	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973720-50973985	T-47D	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973760-50973910	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973720-50973870	HFF-Myc	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973720-50974002	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973760-50973910	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973728-50973980	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50973780-50973930	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973760-50973910	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973820-50973970	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr2:50976420-50976570	Caco-2	colon:	n/a	n/a
38	CTCF	chr2:50973654-50974028	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50978500-50978650	HMEC	breast:	n/a	n/a
41	CTCF	chr2:50973634-50974016	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973800-50973950	HL-60	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973800-50973950	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973760-50973910	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973780-50973930	GM12873	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50926700-50926850	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr2:50973717-50973974	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973780-50973930	AG04449	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50992829-50992879	SK-N-MC	brain:	n/a
2	chr2:50992829-50992879	Hepatocyte	liver:	n/a
3	chr2:50992829-50992879	Hela-S3	cervix:	n/a
4	chr2:50956659-50956709	CMK	blood:	n/a
5	chr2:50992829-50992879	U87	brain:	n/a
6	chr2:50992829-50992879	GM12891	blood:	n/a
7	chr2:50956659-50956709	PFSK-1	brain:	n/a
8	chr2:50956659-50956709	AG09319	gingival:	n/a
9	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
10	chr2:50992829-50992879	NHDF-neo	bronchial:	n/a
11	chr2:50992829-50992879	Caco-2	colon:	n/a
12	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
13	chr2:50992829-50992879	NT2-D1	testis:	n/a
14	chr2:50992829-50992879	HCF	heart:	n/a
15	chr2:50956659-50956709	BE2_C	brain:	n/a
16	chr2:50956659-50956709	MCF-7	breast:	n/a
17	chr2:50992829-50992879	AG04450	lung:	fetal
18	chr2:50992829-50992879	HRE	kidney:	n/a
19	chr2:50992829-50992879	PrEC	prostate:	n/a
20	chr2:50956659-50956709	HAEpiC	amniotic membrane:	n/a
21	chr2:50992829-50992879	AoSMC	blood vessel:	n/a
22	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
23	chr2:50956659-50956709	HEK293	kidney:	embryo
24	chr2:50992829-50992879	IMR90	lung:	fetal
25	chr2:50956659-50956709	LNCaP	prostate:	n/a
26	chr2:50956659-50956709	ProgFib	skin:	n/a
27	chr2:50992829-50992879	HCM	heart:	n/a
28	chr2:50992829-50992879	ProgFib	skin:	n/a
29	chr2:50956659-50956709	GM06990	blood:	n/a
30	chr2:50992829-50992879	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:50992829-50992879	HEK293	kidney:	embryo
32	chr2:50992829-50992879	LNCaP	prostate:	n/a
33	chr2:50992829-50992879	NH-A	brain:	n/a
34	chr2:50956659-50956709	U87	brain:	n/a
35	chr2:50956659-50956709	Jurkat	blood:	n/a
36	chr2:50956659-50956709	PrEC	prostate:	n/a
37	chr2:50992829-50992879	HAEpiC	amniotic membrane:	n/a
38	chr2:50992829-50992879	K562	blood:	n/a
39	chr2:50956659-50956709	Hela-S3	cervix:	n/a
40	chr2:50956659-50956709	HMEC	breast:	n/a
41	chr2:50992829-50992879	PFSK-1	brain:	n/a
42	chr2:50956659-50956709	SAEC	small airway:	n/a
43	chr2:50992829-50992879	PANC-1	pancreas:	n/a
44	chr2:50956659-50956709	NH-A	brain:	n/a
45	chr2:50956659-50956709	NT2-D1	testis:	n/a
46	chr2:50992829-50992879	GM06990	blood:	n/a
47	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
48	chr2:50992829-50992879	RPTEC	kidney:	n/a
49	chr2:50956659-50956709	RPTEC	kidney:	n/a
50	chr2:50992829-50992879	BE2_C	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	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
6	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
7	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
8	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000216191	CpG island

Extended variants
information (count: 2570 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2570 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17501068	chr2:50923733-50923734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544577750	chr2:50923744-50923745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367654760	chr2:50923795-50923796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs698844	chr2:50923850-50923851	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs138204799	chr2:50923863-50923864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs994991	chr2:50923891-50923892	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs377471222	chr2:50923916-50923917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369071822	chr2:50923952-50923953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72887545	chr2:50924005-50924006	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373125123	chr2:50924014-50924015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550797445	chr2:50924044-50924045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530294951	chr2:50924047-50924048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539838619	chr2:50924049-50924050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569344890	chr2:50924059-50924060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143688067	chr2:50924071-50924072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551783760	chr2:50924082-50924083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144136216	chr2:50924089-50924090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148730088	chr2:50924090-50924091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537602490	chr2:50924150-50924151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555966636	chr2:50924196-50924197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567774019	chr2:50924211-50924212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566952499	chr2:50924219-50924220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538389080	chr2:50924224-50924225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555862945	chr2:50924265-50924266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150860603	chr2:50924298-50924299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544641163	chr2:50924324-50924325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113029622	chr2:50924329-50924330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17560229	chr2:50924358-50924359	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191427373	chr2:50924366-50924367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182798054	chr2:50924380-50924381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531426204	chr2:50924417-50924418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187424186	chr2:50924419-50924420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563004361	chr2:50924439-50924440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191967757	chr2:50924501-50924502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184260912	chr2:50924511-50924512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79618071	chr2:50924515-50924516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552596891	chr2:50924516-50924517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527644362	chr2:50924522-50924523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549414968	chr2:50924558-50924559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113582709	chr2:50924603-50924604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571181450	chr2:50924615-50924616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538072664	chr2:50924633-50924634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146593438	chr2:50924646-50924647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527335839	chr2:50924705-50924706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538347015	chr2:50924719-50924720	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs377304677	chr2:50924765-50924766	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553394968	chr2:50924793-50924794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs571946586	chr2:50924804-50924805	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs536212920	chr2:50924829-50924830	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554581995	chr2:50924841-50924842	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:50916200-50923800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:50919200-50929200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:50923800-50924200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:50924200-50924800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr2:50924800-50929800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:50929000-50929200	Enhancers	Brain Hippocampus Middle	brain
8	chr2:50929200-50929600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:50929200-50930000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:50929200-50930400	Weak transcription	Brain Hippocampus Middle	brain
11	chr2:50929400-50929800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:50929600-50930400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:50929800-50930800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:50930000-50935400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:50930400-50930800	Enhancers	Brain Hippocampus Middle	brain
16	chr2:50930400-50934400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr2:50930800-50941400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr2:50934200-50935000	Enhancers	Brain Substantia Nigra	brain
19	chr2:50934400-50935000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:50934400-50935000	Enhancers	Brain Germinal Matrix	brain
21	chr2:50934600-50935000	Enhancers	Fetal Brain Male	brain
22	chr2:50934800-50935000	Enhancers	Brain Anterior Caudate	brain
23	chr2:50935000-50936000	Weak transcription	Brain Anterior Caudate	brain
24	chr2:50935000-50939800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr2:50935000-50947400	Weak transcription	Fetal Brain Male	brain
26	chr2:50935400-50935800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr2:50935400-50936000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:50936000-50936400	Enhancers	Brain Anterior Caudate	brain
29	chr2:50936000-50936400	Enhancers	Pancreas	Pancrea
30	chr2:50937200-50940600	Enhancers	Liver	Liver
31	chr2:50939600-50939800	Enhancers	Fetal Brain Female	brain
32	chr2:50939800-50942000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr2:50939800-50947600	Weak transcription	Fetal Brain Female	brain
34	chr2:50940600-50944800	Weak transcription	Liver	Liver
35	chr2:50941000-50942000	Enhancers	Fetal Kidney	kidney
36	chr2:50941400-50942000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr2:50941600-50945600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:50942000-50943200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr2:50942000-50947000	Weak transcription	Fetal Kidney	kidney
40	chr2:50942000-50947600	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr2:50943200-50944400	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:50944400-50946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:50944800-50945400	Enhancers	Liver	Liver
44	chr2:50945400-50945600	Enhancers	Brain Substantia Nigra	brain
45	chr2:50945400-50945800	Enhancers	Brain Hippocampus Middle	brain
46	chr2:50945400-50946600	Weak transcription	Liver	Liver
47	chr2:50945600-50946000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:50945600-50947400	Weak transcription	Brain Substantia Nigra	brain
49	chr2:50945800-50946000	Enhancers	Brain Anterior Caudate	brain
50	chr2:50945800-50947600	Weak transcription	Brain Hippocampus Middle	brain

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