Variant report

Variant	nsv1004908
Chromosome Location	chr2:50868551-50987144
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	chr2:50952033-50952347	A549	lung:	n/a	n/a
3	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
5	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
6	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
8	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
9	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
12	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
13	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973732-50973965	GM19238	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50902120-50902270	HMEC	breast:	n/a	n/a
17	CTCF	chr2:50902155-50902320	GM12878	blood:	n/a	n/a
18	CTCF	chr2:50902140-50902290	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr2:50902155-50902284	GM13977	blood:	n/a	n/a
20	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
21	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50902046-50902364	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
24	CTCF	chr2:50889610-50889663	GM12891	blood:	n/a	n/a
25	CTCF	chr2:50973780-50973930	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50902100-50902250	HCT-116	colon:	n/a	n/a
27	CTCF	chr2:50973740-50973890	NB4	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973720-50973870	HVMF	connective:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973760-50973910	GM12872	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50902189-50902272	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:50902120-50902270	HepG2	liver:	n/a	n/a
33	CTCF	chr2:50973780-50973930	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973740-50973890	GM12873	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50902146-50902299	GM19238	blood:	n/a	n/a
36	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50902001-50902362	HepG2	liver:	n/a	n/a
38	CTCF	chr2:50973654-50974028	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973740-50973890	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a
41	CTCF	chr2:50902140-50902290	HBMEC	blood vessel:	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	chr2:50902106-50902258	A549	lung:	n/a	n/a
44	CTCF	chr2:50973720-50973870	AoAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973800-50973950	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50902173-50902283	HepG2	liver:	n/a	n/a
47	CTCF	chr2:50973780-50973930	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50902140-50902290	GM12871	blood:	n/a	n/a
49	CTCF	chr2:50973740-50973890	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50884693-50884743	HRPEpiC	eye:	n/a
2	chr2:50876837-50876887	HRE	kidney:	n/a
3	chr2:50884252-50884302	HCPEpiC	choroid plexus:	n/a
4	chr2:50884252-50884302	GM19239	blood:	n/a
5	chr2:50884693-50884743	AG10803	skin:	n/a
6	chr2:50884252-50884302	HUVEC	blood vessel:	n/a
7	chr2:50956659-50956709	SK-N-SH	brain:	n/a
8	chr2:50884252-50884302	ProgFib	skin:	n/a
9	chr2:50884252-50884302	NHBE	bronchial:	n/a
10	chr2:50876837-50876887	HepG2	liver:	n/a
11	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
12	chr2:50956659-50956709	Caco-2	colon:	n/a
13	chr2:50956659-50956709	AG04450	lung:	fetal
14	chr2:50956659-50956709	GM06990	blood:	n/a
15	chr2:50884693-50884743	HCM	heart:	n/a
16	chr2:50884252-50884302	SK-N-SH_RA	brain:	n/a
17	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
18	chr2:50884693-50884743	HCPEpiC	choroid plexus:	n/a
19	chr2:50876837-50876887	SK-N-SH	brain:	n/a
20	chr2:50884252-50884302	PFSK-1	brain:	n/a
21	chr2:50956659-50956709	NH-A	brain:	n/a
22	chr2:50884252-50884302	HCM	heart:	n/a
23	chr2:50956659-50956709	HRPEpiC	eye:	n/a
24	chr2:50876837-50876887	SK-N-SH_RA	brain:	n/a
25	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
26	chr2:50884693-50884743	HRCEpiC	kidney:	n/a
27	chr2:50956659-50956709	Hela-S3	cervix:	n/a
28	chr2:50884693-50884743	RPTEC	kidney:	n/a
29	chr2:50956659-50956709	PFSK-1	brain:	n/a
30	chr2:50956659-50956709	AoSMC	blood vessel:	n/a
31	chr2:50876837-50876887	GM12892	blood:	n/a
32	chr2:50876837-50876887	AG04450	lung:	fetal
33	chr2:50884693-50884743	Hepatocyte	liver:	n/a
34	chr2:50884252-50884302	MCF-7	breast:	n/a
35	chr2:50884693-50884743	NT2-D1	testis:	n/a
36	chr2:50884252-50884302	HRPEpiC	eye:	n/a
37	chr2:50884252-50884302	GM12878	blood:	n/a
38	chr2:50956659-50956709	H1-hESC	embryonic stem cell:	embryo
39	chr2:50956659-50956709	HNPCEpiC	eye:	n/a
40	chr2:50956659-50956709	HEK293	kidney:	embryo
41	chr2:50884252-50884302	IMR90	lung:	fetal
42	chr2:50884252-50884302	GM12892	blood:	n/a
43	chr2:50884252-50884302	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:50876837-50876887	SKMC	muscle:	n/a
45	chr2:50884693-50884743	LNCaP	prostate:	n/a
46	chr2:50884252-50884302	GM12891	blood:	n/a
47	chr2:50876837-50876887	HCT-116	colon:	n/a
48	chr2:50876837-50876887	Hela-S3	cervix:	n/a
49	chr2:50876837-50876887	RPTEC	kidney:	n/a
50	chr2:50884693-50884743	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
4	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
5	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
6	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
9	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
10	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
11	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
12	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:

Variant related genes	Relation type
ENSG00000216191	TF binding region
NRXN1	TF binding region
ENSG00000216191	CpG island
NRXN1	CpG island
ENSG00000179915	chromatin interactions
ENSG00000216191	chromatin interactions

Extended variants
information (count: 4135 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4135 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2194387	chr2:50868551-50868552	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539946244	chr2:50868594-50868595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557921584	chr2:50868659-50868660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572912004	chr2:50868668-50868669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540226895	chr2:50868669-50868670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371962027	chr2:50868684-50868685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573975458	chr2:50868715-50868716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544541736	chr2:50868719-50868720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563116489	chr2:50868738-50868739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138406891	chr2:50868753-50868754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575377775	chr2:50868755-50868756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142405032	chr2:50868805-50868806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527329279	chr2:50868808-50868809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138871580	chr2:50868809-50868810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567599610	chr2:50868822-50868823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531655198	chr2:50868829-50868830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549780637	chr2:50868831-50868832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571423194	chr2:50868858-50868859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538415509	chr2:50868873-50868874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183414650	chr2:50868875-50868876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187770380	chr2:50868876-50868877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149400525	chr2:50868896-50868897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533961764	chr2:50868901-50868902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555356061	chr2:50868910-50868911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143842222	chr2:50868925-50868926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72885646	chr2:50868932-50868933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556537041	chr2:50868988-50868989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578154229	chr2:50868997-50868998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545268248	chr2:50869026-50869027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560316979	chr2:50869042-50869043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527365073	chr2:50869131-50869132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542712453	chr2:50869137-50869138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559826131	chr2:50869151-50869152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192444053	chr2:50869273-50869274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182463593	chr2:50869290-50869291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531285835	chr2:50869354-50869355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72885647	chr2:50869365-50869366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs565027439	chr2:50869372-50869373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187591164	chr2:50869392-50869393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148160506	chr2:50869434-50869435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528561652	chr2:50869438-50869439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113578970	chr2:50869454-50869455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4518000	chr2:50869459-50869460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs369969811	chr2:50869544-50869545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192925130	chr2:50869597-50869598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78934893	chr2:50869616-50869617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141565166	chr2:50869660-50869661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78695979	chr2:50869691-50869692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537838778	chr2:50869736-50869737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540540306	chr2:50869738-50869739	Weak transcription	n/a	n/a	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:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50868400-50868600	Enhancers	Fetal Brain Male	brain
2	chr2:50868600-50869000	Enhancers	Fetal Muscle Leg	muscle
3	chr2:50868600-50872200	Weak transcription	Fetal Brain Male	brain
4	chr2:50869000-50875600	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:50872200-50877800	Enhancers	Fetal Brain Male	brain
6	chr2:50872600-50873200	Enhancers	Fetal Brain Female	brain
7	chr2:50872800-50873400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:50873000-50873200	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:50873000-50873400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:50873000-50873400	Enhancers	Brain Substantia Nigra	brain
11	chr2:50873200-50874000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:50873200-50875600	Weak transcription	Fetal Brain Female	brain
13	chr2:50873200-50875800	Weak transcription	Fetal Kidney	kidney
14	chr2:50873400-50874800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:50873400-50875400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:50873400-50875400	Weak transcription	Brain Substantia Nigra	brain
17	chr2:50873600-50873800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:50873800-50876800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:50874000-50875600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr2:50874800-50878000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr2:50875400-50876000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr2:50875400-50876000	Enhancers	Brain Substantia Nigra	brain
24	chr2:50875400-50877800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:50875600-50876000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:50875600-50876000	Enhancers	Brain Hippocampus Middle	brain
27	chr2:50875600-50876000	Enhancers	Fetal Brain Female	brain
28	chr2:50875600-50876000	Enhancers	Fetal Muscle Leg	muscle
29	chr2:50875600-50876200	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:50875600-50878000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:50875800-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:50875800-50877600	Enhancers	HSMMtube	muscle
33	chr2:50875800-50878000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:50876000-50876400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr2:50876000-50877000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr2:50876000-50877000	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:50876000-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr2:50876000-50877000	Enhancers	NHEK	skin
39	chr2:50876000-50878800	Weak transcription	Brain Hippocampus Middle	brain
40	chr2:50876000-50878800	Weak transcription	Brain Substantia Nigra	brain
41	chr2:50876000-50878800	Weak transcription	Fetal Brain Female	brain
42	chr2:50876200-50879200	Weak transcription	Brain Cingulate Gyrus	brain
43	chr2:50876400-50878200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr2:50876400-50879800	Enhancers	HMEC	breast
45	chr2:50876600-50877200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:50876600-50877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:50876600-50877800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr2:50876600-50877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:50876800-50877400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:50876800-50877400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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