Variant report

Variant	nsv949284
Chromosome Location	chr2:50946373-51080824
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	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
4	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
5	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
6	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
7	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
11	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
12	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
14	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
15	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
17	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
18	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
19	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
20	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
21	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:50973780-50973930	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973717-50973974	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973740-50973931	GM10266	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
26	CTCF	chr2:50973100-50973250	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
28	CTCF	chr2:50973800-50973950	HL-60	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973740-50973890	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973634-50974016	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	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	chr2:50973622-50974108	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973740-50973890	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973739-50973958	LNCaP	prostate:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973760-50973910	HCFaa	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973820-50973970	HFF-Myc	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973700-50973850	NHDF-neo	bronchial:	n/a	chr2:50973841-50973849
40	CTCF	chr2:50973740-50973890	NB4	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973760-50973910	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973780-50973930	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973780-50973930	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973760-50973910	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
47	CTCF	chr2:50973720-50973870	HVMF	connective:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973752-50973913	GM10248	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973572-50973669	Gliobla	brain:	n/a	n/a
50	CTCF	chr2:50973740-50973890	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	NB4	blood:	n/a
2	chr2:50956659-50956709	NB4	blood:	n/a
3	chr2:51001003-51001053	GM06990	blood:	n/a
4	chr2:50992829-50992879	SK-N-SH	brain:	n/a
5	chr2:51065673-51065723	HUVEC	blood vessel:	n/a
6	chr2:51074881-51074931	MCF-7	breast:	n/a
7	chr2:51056822-51056872	ProgFib	skin:	n/a
8	chr2:51065673-51065723	HepG2	liver:	n/a
9	chr2:51057218-51057268	HCF	heart:	n/a
10	chr2:51056822-51056872	SK-N-SH_RA	brain:	n/a
11	chr2:51057218-51057268	LNCaP	prostate:	n/a
12	chr2:51074881-51074931	LNCaP	prostate:	n/a
13	chr2:50992829-50992879	AG04450	lung:	fetal
14	chr2:51057218-51057268	H1-hESC	embryonic stem cell:	embryo
15	chr2:51056822-51056872	HEK293	kidney:	embryo
16	chr2:50992829-50992879	SK-N-SH_RA	brain:	n/a
17	chr2:51056884-51056934	AG09319	gingival:	n/a
18	chr2:51056822-51056872	GM12892	blood:	n/a
19	chr2:51056884-51056934	AG10803	skin:	n/a
20	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
21	chr2:51074881-51074931	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:51056884-51056934	AoSMC	blood vessel:	n/a
23	chr2:50956659-50956709	Hela-S3	cervix:	n/a
24	chr2:51074939-51074989	Hepatocyte	liver:	n/a
25	chr2:50956659-50956709	NT2-D1	testis:	n/a
26	chr2:51056884-51056934	HCF	heart:	n/a
27	chr2:51056884-51056934	U87	brain:	n/a
28	chr2:51074881-51074931	HCT-116	colon:	n/a
29	chr2:50956659-50956709	GM12892	blood:	n/a
30	chr2:50992829-50992879	IMR90	lung:	fetal
31	chr2:51001003-51001053	ProgFib	skin:	n/a
32	chr2:51001003-51001053	HCPEpiC	choroid plexus:	n/a
33	chr2:51057548-51057598	HMEC	breast:	n/a
34	chr2:51057548-51057598	IMR90	lung:	fetal
35	chr2:51074939-51074989	SK-N-SH_RA	brain:	n/a
36	chr2:51074939-51074989	HEEpiC	esophagus:	n/a
37	chr2:51057548-51057598	HepG2	liver:	n/a
38	chr2:51074881-51074931	Jurkat	blood:	n/a
39	chr2:51057548-51057598	RPTEC	kidney:	n/a
40	chr2:51001003-51001053	MCF10A-Er-Src	breast:	n/a
41	chr2:51057548-51057598	GM12892	blood:	n/a
42	chr2:51056822-51056872	AG10803	skin:	n/a
43	chr2:51056822-51056872	HRPEpiC	eye:	n/a
44	chr2:50956659-50956709	CMK	blood:	n/a
45	chr2:51074881-51074931	PFSK-1	brain:	n/a
46	chr2:51065673-51065723	AG09319	gingival:	n/a
47	chr2:51074881-51074931	BJ	skin:	n/a
48	chr2:51074939-51074989	U87	brain:	n/a
49	chr2:51056822-51056872	GM12891	blood:	n/a
50	chr2:51056822-51056872	Caco-2	colon:	n/a

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

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

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

Extended variants
information (count: 4696 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4696 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17040976	chr2:50946373-50946374	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576413339	chr2:50946458-50946459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535211002	chr2:50946460-50946461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187218966	chr2:50946514-50946515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574462701	chr2:50946530-50946531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535150259	chr2:50946535-50946536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556916097	chr2:50946539-50946540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574850096	chr2:50946580-50946581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545707167	chr2:50946581-50946582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577561197	chr2:50946630-50946631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564010738	chr2:50946665-50946666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112113177	chr2:50946676-50946677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193111141	chr2:50946724-50946725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375244039	chr2:50946771-50946772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546402986	chr2:50946786-50946787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143529042	chr2:50946791-50946792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183927528	chr2:50946792-50946793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546109753	chr2:50946824-50946825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201052080	chr2:50946825-50946826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555810116	chr2:50946830-50946831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541918147	chr2:50946831-50946832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373306297	chr2:50946839-50946840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575518816	chr2:50946842-50946843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76214245	chr2:50946894-50946895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552934099	chr2:50946897-50946898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151215800	chr2:50946937-50946938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528734652	chr2:50946939-50946940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115077801	chr2:50946956-50946957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553717366	chr2:50946965-50946966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140464694	chr2:50946991-50946992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17501747	chr2:50947044-50947045	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556745431	chr2:50947094-50947095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540673160	chr2:50947121-50947122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375233195	chr2:50947127-50947128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55703245	chr2:50947149-50947150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187660950	chr2:50947179-50947180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11125324	chr2:50947214-50947215	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs150394155	chr2:50947235-50947236	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572799551	chr2:50947288-50947289	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs560897991	chr2:50947379-50947380	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs367547424	chr2:50947400-50947401	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540108983	chr2:50947401-50947402	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs113169764	chr2:50947418-50947419	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573721909	chr2:50947434-50947435	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs542333034	chr2:50947445-50947446	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs111479168	chr2:50947502-50947503	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs372198910	chr2:50947510-50947511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs858942	chr2:50947512-50947513	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563020685	chr2:50947520-50947521	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs546212882	chr2:50947529-50947530	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr2:50942000-50947000	Weak transcription	Fetal Kidney	kidney
5	chr2:50942000-50947600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:50944400-50946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:50945400-50946600	Weak transcription	Liver	Liver
8	chr2:50945600-50947400	Weak transcription	Brain Substantia Nigra	brain
9	chr2:50945800-50947600	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:50946000-50947200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:50946000-50948000	Weak transcription	Brain Anterior Caudate	brain
12	chr2:50946600-50948600	Enhancers	Liver	Liver
13	chr2:50946800-50947200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:50947000-50947600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:50947000-50947600	Enhancers	Fetal Kidney	kidney
16	chr2:50947000-50948400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:50947000-50948800	Enhancers	Brain Angular Gyrus	brain
18	chr2:50947200-50947600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr2:50947200-50947800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:50947200-50948400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:50947200-50948600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:50947200-50948600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:50947400-50947600	Enhancers	Fetal Brain Male	brain
24	chr2:50947400-50947800	Enhancers	Brain Substantia Nigra	brain
25	chr2:50947400-50948200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:50947400-50948400	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr2:50947400-50948600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:50947400-50948600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:50947400-50948600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:50947400-50948600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:50947400-50948800	Enhancers	Brain Germinal Matrix	brain
32	chr2:50947600-50948000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr2:50947600-50948200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:50947600-50948200	Weak transcription	Fetal Brain Male	brain
35	chr2:50947600-50948600	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr2:50947600-50948800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:50947600-50948800	Enhancers	Brain Hippocampus Middle	brain
38	chr2:50947600-50948800	Enhancers	Fetal Brain Female	brain
39	chr2:50947600-50950800	Weak transcription	Fetal Kidney	kidney
40	chr2:50947800-50948000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr2:50947800-50948400	Enhancers	Fetal Muscle Leg	muscle
42	chr2:50947800-50948600	Enhancers	Brain Cingulate Gyrus	brain
43	chr2:50947800-50948600	Enhancers	Fetal Stomach	stomach
44	chr2:50947800-50949800	Weak transcription	Brain Substantia Nigra	brain
45	chr2:50948000-50948200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:50948000-50948200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr2:50948000-50948400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:50948000-50948600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:50948000-50948800	Enhancers	Brain Anterior Caudate	brain
50	chr2:50948200-50948400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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