Variant report

Variant	nsv948782
Chromosome Location	chr2:50897511-51164552
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	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
5	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
7	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
8	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
9	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
10	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
12	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
15	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
18	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
19	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
22	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
23	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
24	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
25	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
26	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
27	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
28	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
30	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
31	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
32	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
33	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
34	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
35	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
36	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
37	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
38	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
39	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
40	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:51099780-51099930	HMEC	breast:	n/a	n/a
42	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:51099820-51099970	HAc	cerebellar:	n/a	n/a
46	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr2:50902091-50902331	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973800-50973950	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50902140-50902290	GM12871	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51074881-51074931	HEEpiC	esophagus:	n/a
2	chr2:51074881-51074931	HEEpiC	esophagus:	n/a
3	chr2:51001003-51001053	ECC-1	luminal epithelium:	n/a
4	chr2:51057218-51057268	K562	blood:	n/a
5	chr2:51074939-51074989	HRPEpiC	eye:	n/a
6	chr2:51056884-51056934	Jurkat	blood:	n/a
7	chr2:51057218-51057268	ovcar-3	ovarian:	n/a
8	chr2:51001003-51001053	HepG2	liver:	n/a
9	chr2:51065673-51065723	SAEC	small airway:	n/a
10	chr2:51065673-51065723	NB4	blood:	n/a
11	chr2:50956659-50956709	GM12892	blood:	n/a
12	chr2:51057218-51057268	Hepatocyte	liver:	n/a
13	chr2:50992829-50992879	NT2-D1	testis:	n/a
14	chr2:50956659-50956709	NH-A	brain:	n/a
15	chr2:51056822-51056872	NH-A	brain:	n/a
16	chr2:51057548-51057598	NT2-D1	testis:	n/a
17	chr2:51056822-51056872	GM12892	blood:	n/a
18	chr2:51074939-51074989	HEEpiC	esophagus:	n/a
19	chr2:51057218-51057268	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:51056884-51056934	PANC-1	pancreas:	n/a
21	chr2:50956659-50956709	HMEC	breast:	n/a
22	chr2:51074939-51074989	Hela-S3	cervix:	n/a
23	chr2:50956659-50956709	IMR90	lung:	fetal
24	chr2:51074939-51074989	AG10803	skin:	n/a
25	chr2:51074939-51074989	NHBE	bronchial:	n/a
26	chr2:50956659-50956709	BJ	skin:	n/a
27	chr2:51074881-51074931	SAEC	small airway:	n/a
28	chr2:51057218-51057268	HUVEC	blood vessel:	n/a
29	chr2:51074881-51074931	HepG2	liver:	n/a
30	chr2:51074939-51074989	NH-A	brain:	n/a
31	chr2:51057218-51057268	Caco-2	colon:	n/a
32	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
33	chr2:51056822-51056872	HCF	heart:	n/a
34	chr2:51057548-51057598	NHDF-neo	bronchial:	n/a
35	chr2:51001003-51001053	K562	blood:	n/a
36	chr2:51074881-51074931	AoSMC	blood vessel:	n/a
37	chr2:51057218-51057268	T-47D	breast:	n/a
38	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
39	chr2:51057218-51057268	HAEpiC	amniotic membrane:	n/a
40	chr2:50956659-50956709	GM12878	blood:	n/a
41	chr2:51057218-51057268	RPTEC	kidney:	n/a
42	chr2:51074881-51074931	SK-N-MC	brain:	n/a
43	chr2:51056884-51056934	BE2_C	brain:	n/a
44	chr2:51001003-51001053	LNCaP	prostate:	n/a
45	chr2:50956659-50956709	HEK293	kidney:	embryo
46	chr2:51057218-51057268	HNPCEpiC	eye:	n/a
47	chr2:51001003-51001053	NHBE	bronchial:	n/a
48	chr2:51065673-51065723	NT2-D1	testis:	n/a
49	chr2:51074881-51074931	MCF-7	breast:	n/a
50	chr2:51074939-51074989	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
2	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
3	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
4	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
5	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
6	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
7	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
8	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
9	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
10	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
11	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
12	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
13	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
14	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
15	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
16	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
17	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
18	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
19	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
20	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
21	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
22	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island
ENSG00000216191	chromatin interactions

Extended variants
information (count: 9319 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:9319 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11883891	chr2:50897511-50897512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539508431	chr2:50897541-50897542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557822587	chr2:50897544-50897545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35327502	chr2:50897545-50897546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386390170	chr2:50897547-50897548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72533912	chr2:50897548-50897549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3085886	chr2:50897549-50897550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189549154	chr2:50897597-50897598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182612833	chr2:50897599-50897600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148120103	chr2:50897602-50897603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573811340	chr2:50897689-50897690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544397634	chr2:50897710-50897711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562514603	chr2:50897734-50897735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185592287	chr2:50897744-50897745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552236994	chr2:50897789-50897790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564189814	chr2:50897798-50897799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190054162	chr2:50897808-50897809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141869062	chr2:50897862-50897863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368706150	chr2:50897882-50897883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546549652	chr2:50897913-50897914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183831483	chr2:50897970-50897971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576014042	chr2:50897979-50897980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535749485	chr2:50897984-50897985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551173740	chr2:50898011-50898012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150669954	chr2:50898022-50898023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188366525	chr2:50898062-50898063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78398101	chr2:50898077-50898078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552127184	chr2:50898115-50898116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559215994	chr2:50898128-50898129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528139090	chr2:50898136-50898137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10203342	chr2:50898228-50898229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534557509	chr2:50898255-50898256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548003597	chr2:50898286-50898287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567874298	chr2:50898295-50898296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555016225	chr2:50898383-50898384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573901437	chr2:50898403-50898404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138913641	chr2:50898414-50898415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547047587	chr2:50898488-50898489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74478135	chr2:50898496-50898497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116698492	chr2:50898521-50898522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537427173	chr2:50898523-50898524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577760360	chr2:50898576-50898577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193257258	chr2:50898691-50898692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114213351	chr2:50898720-50898721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528520075	chr2:50898721-50898722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556070568	chr2:50898725-50898726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561902486	chr2:50898730-50898731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77387730	chr2:50898733-50898734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550649442	chr2:50898799-50898800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9309185	chr2:50898816-50898817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:110)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD

Chromatin state (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50890400-50899200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:50899200-50899600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:50899200-50899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:50899600-50899800	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
7	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
8	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
10	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
15	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
18	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
20	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
27	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
31	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
40	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr2:50916000-50918600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:50916000-50918800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:50916200-50923800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:50917600-50917800	Enhancers	Brain Hippocampus Middle	brain
47	chr2:50917600-50918000	Weak transcription	Brain Substantia Nigra	brain
48	chr2:50917600-50918400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr2:50917800-50918400	Enhancers	Brain Angular Gyrus	brain
50	chr2:50917800-50918600	Enhancers	Brain Anterior Caudate	brain

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