Variant report

Variant	nsv1009157
Chromosome Location	chr2:50894934-51140228
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	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:50955596-50955702	K562	blood:	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	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
5	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
6	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
8	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
12	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
13	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
14	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
15	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
16	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
18	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
20	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
21	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
22	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
24	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
26	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
27	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
29	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
30	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
31	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
33	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
34	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
35	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
36	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:50902100-50902250	HCT-116	colon:	n/a	n/a
38	CTCF	chr2:50902155-50902284	GM13977	blood:	n/a	n/a
39	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973100-50973250	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr2:50902120-50902270	GM12866	blood:	n/a	n/a
42	CTCF	chr2:50973780-50973930	HRPEpiC	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973780-50973930	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973760-50973923	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
46	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973760-50973910	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973581-50974034	IMR90	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51074939-51074989	NH-A	brain:	n/a
2	chr2:50992829-50992879	SAEC	small airway:	n/a
3	chr2:51057218-51057268	AG09319	gingival:	n/a
4	chr2:51065673-51065723	NHDF-neo	bronchial:	n/a
5	chr2:51065673-51065723	AG04449	skin:	fetal
6	chr2:50956659-50956709	NT2-D1	testis:	n/a
7	chr2:51057218-51057268	NB4	blood:	n/a
8	chr2:51057218-51057268	HCPEpiC	choroid plexus:	n/a
9	chr2:50992829-50992879	HEEpiC	esophagus:	n/a
10	chr2:51057548-51057598	HRCEpiC	kidney:	n/a
11	chr2:51001003-51001053	BE2_C	brain:	n/a
12	chr2:51057218-51057268	NHBE	bronchial:	n/a
13	chr2:51074939-51074989	MCF10A-Er-Src	breast:	n/a
14	chr2:51056822-51056872	AoSMC	blood vessel:	n/a
15	chr2:51056822-51056872	ovcar-3	ovarian:	n/a
16	chr2:51074881-51074931	RPTEC	kidney:	n/a
17	chr2:51056822-51056872	GM19239	blood:	n/a
18	chr2:51056822-51056872	AG04450	lung:	fetal
19	chr2:51057218-51057268	AG10803	skin:	n/a
20	chr2:51074939-51074989	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:51074881-51074931	Hepatocyte	liver:	n/a
22	chr2:50992829-50992879	HepG2	liver:	n/a
23	chr2:51074881-51074931	SKMC	muscle:	n/a
24	chr2:51056822-51056872	NB4	blood:	n/a
25	chr2:50992829-50992879	HCT-116	colon:	n/a
26	chr2:51057548-51057598	HCT-116	colon:	n/a
27	chr2:51057548-51057598	U87	brain:	n/a
28	chr2:50992829-50992879	PFSK-1	brain:	n/a
29	chr2:51074881-51074931	HMEC	breast:	n/a
30	chr2:51065673-51065723	HIPEpiC	eye:	n/a
31	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
32	chr2:51057218-51057268	BJ	skin:	n/a
33	chr2:51074881-51074931	HNPCEpiC	eye:	n/a
34	chr2:51074939-51074989	HL-60	blood:	n/a
35	chr2:51056822-51056872	AG04449	skin:	fetal
36	chr2:51074939-51074989	HRCEpiC	kidney:	n/a
37	chr2:51057548-51057598	PrEC	prostate:	n/a
38	chr2:50956659-50956709	CMK	blood:	n/a
39	chr2:51001003-51001053	HNPCEpiC	eye:	n/a
40	chr2:51056884-51056934	Hepatocyte	liver:	n/a
41	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
42	chr2:51001003-51001053	U87	brain:	n/a
43	chr2:50992829-50992879	LNCaP	prostate:	n/a
44	chr2:51074881-51074931	AG09319	gingival:	n/a
45	chr2:51074939-51074989	AoSMC	blood vessel:	n/a
46	chr2:51065673-51065723	T-47D	breast:	n/a
47	chr2:51056884-51056934	MCF10A-Er-Src	breast:	n/a
48	chr2:51074939-51074989	HRE	kidney:	n/a
49	chr2:51065673-51065723	GM12878	blood:	n/a
50	chr2:51001003-51001053	SK-N-MC	brain:	n/a

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

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: 8401 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:8401 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1401178	chr2:50894934-50894935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543659521	chr2:50894960-50894961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372746633	chr2:50894973-50894974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532239924	chr2:50894983-50894984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs698843	chr2:50894997-50894998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547071603	chr2:50895010-50895011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558948658	chr2:50895016-50895017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11884611	chr2:50895038-50895039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191979284	chr2:50895094-50895095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569860047	chr2:50895108-50895109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546335403	chr2:50895143-50895144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537303740	chr2:50895159-50895160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184268858	chr2:50895182-50895183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565761978	chr2:50895216-50895217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189205630	chr2:50895220-50895221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554305604	chr2:50895254-50895255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572516511	chr2:50895255-50895256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147954626	chr2:50895287-50895288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193083312	chr2:50895364-50895365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11902159	chr2:50895387-50895388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs544057965	chr2:50895418-50895419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565371698	chr2:50895423-50895424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184671928	chr2:50895428-50895429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540770980	chr2:50895522-50895523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188989667	chr2:50895536-50895537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140346596	chr2:50895572-50895573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs858930	chr2:50895613-50895614	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs79040017	chr2:50895623-50895624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563265586	chr2:50895640-50895641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181310696	chr2:50895653-50895654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144178496	chr2:50895693-50895694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184024114	chr2:50895705-50895706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377044882	chr2:50895764-50895765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189154439	chr2:50895765-50895766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151173399	chr2:50895766-50895767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140164942	chr2:50895797-50895798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374615838	chr2:50895812-50895813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149931575	chr2:50895821-50895822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs864551	chr2:50895837-50895838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554679733	chr2:50895846-50895847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570015468	chr2:50895849-50895850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537369953	chr2:50895895-50895896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559197207	chr2:50895927-50895928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577062653	chr2:50895939-50895940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144978842	chr2:50896031-50896032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553102808	chr2:50896059-50896060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181687014	chr2:50896064-50896065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541894531	chr2:50896071-50896072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563166139	chr2:50896075-50896076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530523443	chr2:50896151-50896152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	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:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50890400-50899200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:50890800-50895000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:50894800-50895800	Enhancers	Brain Angular Gyrus	brain
4	chr2:50895000-50895200	Enhancers	Brain Germinal Matrix	brain
5	chr2:50895000-50895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:50895000-50895800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:50895200-50896200	Enhancers	Brain Substantia Nigra	brain
8	chr2:50895600-50896000	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:50895800-50896000	Enhancers	Brain Germinal Matrix	brain
10	chr2:50896000-50896400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:50899200-50899600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:50899200-50899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:50899600-50899800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
16	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
17	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
19	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
24	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
27	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
29	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
36	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
40	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
49	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell

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