Variant report

Variant	nsv933327
Chromosome Location	chr2:51049645-51180620
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	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
5	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
6	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
7	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
8	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
9	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
10	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
11	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
12	CEBPB	chr2:51180081-51180588	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
13	CEBPB	chr2:51179698-51180729	Hela-S3	cervix:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
14	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
15	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
16	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
18	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:51180165-51180469	A549	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
20	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
22	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
23	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
24	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
25	CEBPB	chr2:51179690-51180699	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
26	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
27	CEBPB	chr2:51180205-51180442	H1-hESC	embryonic stem cell:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
28	CEBPB	chr2:51179722-51180770	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
29	CEBPB	chr2:51180217-51180418	K562	blood:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
30	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
31	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
32	CEBPB	chr2:51180127-51180593	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
33	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
34	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
35	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
36	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
37	CHD2	chr2:51179784-51180498	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr2:51164960-51165110	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr2:51099780-51099930	HEK293	kidney:	n/a	n/a
40	CTCF	chr2:51099740-51099890	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:51099820-51099970	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr2:51099800-51099950	Caco-2	colon:	n/a	n/a
43	CTCF	chr2:51099780-51099930	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:51099689-51099932	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr2:51099820-51099970	BE2_C	brain:	n/a	n/a
46	CTCF	chr2:51099820-51099970	SAEC	small airway:	n/a	n/a
47	CTCF	chr2:51159644-51159672	GM13977	blood:	n/a	n/a
48	CTCF	chr2:51099780-51099930	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr2:51099842-51099897	LNCaP	prostate:	n/a	n/a
50	CTCF	chr2:51099780-51099930	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51057548-51057598	T-47D	breast:	n/a
2	chr2:51074939-51074989	HIPEpiC	eye:	n/a
3	chr2:51074881-51074931	Hepatocyte	liver:	n/a
4	chr2:51056822-51056872	NT2-D1	testis:	n/a
5	chr2:51065673-51065723	Hela-S3	cervix:	n/a
6	chr2:51057218-51057268	NT2-D1	testis:	n/a
7	chr2:51074939-51074989	HEK293	kidney:	embryo
8	chr2:51074939-51074989	HRE	kidney:	n/a
9	chr2:51065673-51065723	IMR90	lung:	fetal
10	chr2:51057548-51057598	HUVEC	blood vessel:	n/a
11	chr2:51056822-51056872	LNCaP	prostate:	n/a
12	chr2:51056884-51056934	NHDF-neo	bronchial:	n/a
13	chr2:51074939-51074989	IMR90	lung:	fetal
14	chr2:51057218-51057268	MCF-7	breast:	n/a
15	chr2:51057218-51057268	T-47D	breast:	n/a
16	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
17	chr2:51057218-51057268	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:51074881-51074931	HRCEpiC	kidney:	n/a
19	chr2:51074939-51074989	HepG2	liver:	n/a
20	chr2:51056822-51056872	AG04449	skin:	fetal
21	chr2:51074939-51074989	GM12892	blood:	n/a
22	chr2:51057218-51057268	Jurkat	blood:	n/a
23	chr2:51056884-51056934	SAEC	small airway:	n/a
24	chr2:51056822-51056872	HRCEpiC	kidney:	n/a
25	chr2:51065673-51065723	BE2_C	brain:	n/a
26	chr2:51057218-51057268	LNCaP	prostate:	n/a
27	chr2:51074881-51074931	HepG2	liver:	n/a
28	chr2:51056884-51056934	AG04449	skin:	fetal
29	chr2:51057548-51057598	IMR90	lung:	fetal
30	chr2:51056822-51056872	PANC-1	pancreas:	n/a
31	chr2:51057218-51057268	AG04450	lung:	fetal
32	chr2:51056884-51056934	GM06990	blood:	n/a
33	chr2:51065673-51065723	HAEpiC	amniotic membrane:	n/a
34	chr2:51057548-51057598	HIPEpiC	eye:	n/a
35	chr2:51065673-51065723	NT2-D1	testis:	n/a
36	chr2:51074881-51074931	HL-60	blood:	n/a
37	chr2:51065673-51065723	HCPEpiC	choroid plexus:	n/a
38	chr2:51065673-51065723	HMEC	breast:	n/a
39	chr2:51056884-51056934	AG04450	lung:	fetal
40	chr2:51074881-51074931	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:51057548-51057598	Hela-S3	cervix:	n/a
42	chr2:51057218-51057268	HIPEpiC	eye:	n/a
43	chr2:51056822-51056872	Jurkat	blood:	n/a
44	chr2:51065673-51065723	SK-N-SH_RA	brain:	n/a
45	chr2:51056884-51056934	GM19239	blood:	n/a
46	chr2:51056884-51056934	NB4	blood:	n/a
47	chr2:51074881-51074931	HUVEC	blood vessel:	n/a
48	chr2:51074881-51074931	GM19239	blood:	n/a
49	chr2:51057218-51057268	SAEC	small airway:	n/a
50	chr2:51056884-51056934	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
2	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
3	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
4	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
5	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
6	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
7	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
8	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
9	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
10	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
11	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
12	chr2:51144781..51146893-chr2:51147491..51149076,2	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
ENSG00000216011	TF binding region
ENSG00000238165	CpG island
ENSG00000216011	CpG island

Extended variants
information (count: 4967 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4967 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77480560	chr2:51049698-51049699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72837094	chr2:51049767-51049768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs559108562	chr2:51049780-51049781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117046685	chr2:51049807-51049808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139909424	chr2:51049830-51049831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559824372	chr2:51049881-51049882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574871171	chr2:51049890-51049891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182793162	chr2:51049950-51049951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563745706	chr2:51049953-51049954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367655644	chr2:51049969-51049970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143802016	chr2:51050043-51050044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187118692	chr2:51050091-51050092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564299825	chr2:51050095-51050096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528324070	chr2:51050143-51050144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75444794	chr2:51050170-51050171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115658473	chr2:51050174-51050175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528823454	chr2:51050199-51050200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78416992	chr2:51050205-51050206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547970758	chr2:51050234-51050235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369967199	chr2:51050239-51050240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568565473	chr2:51050245-51050246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147278866	chr2:51050249-51050250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139730908	chr2:51050265-51050266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571021875	chr2:51050296-51050297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9753040	chr2:51050302-51050303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs76299584	chr2:51050378-51050379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575233853	chr2:51050443-51050444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542199537	chr2:51050490-51050491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557402043	chr2:51050503-51050504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575752214	chr2:51050511-51050512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546277533	chr2:51050528-51050529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557314432	chr2:51050569-51050570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564449331	chr2:51050657-51050658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528271601	chr2:51050659-51050660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540069004	chr2:51050673-51050674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192327787	chr2:51050674-51050675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529153549	chr2:51050682-51050683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375634548	chr2:51050727-51050728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184346998	chr2:51050787-51050788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149828418	chr2:51050788-51050789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532810482	chr2:51050805-51050806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539726012	chr2:51050810-51050811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375694705	chr2:51050889-51050890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs67413472	chr2:51050899-51050900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566460326	chr2:51050929-51050930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535191824	chr2:51050934-51050935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553295430	chr2:51051004-51051005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190672531	chr2:51051005-51051006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536148046	chr2:51051008-51051009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565383722	chr2:51051053-51051054	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
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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51041400-51051800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:51048800-51050000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:51048800-51056800	Weak transcription	Brain Germinal Matrix	brain
4	chr2:51050000-51051000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:51050200-51050400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:51050400-51051600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:51051600-51052800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:51051800-51052000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:51052000-51052400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:51052400-51054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:51053000-51058600	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:51054000-51054400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:51054400-51057400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:51056800-51057600	Enhancers	Fetal Brain Male	brain
15	chr2:51056800-51057800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:51056800-51057800	Enhancers	Fetal Brain Female	brain
17	chr2:51056800-51059800	Enhancers	Brain Germinal Matrix	brain
18	chr2:51056800-51060000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr2:51057200-51057400	Enhancers	Brain Anterior Caudate	brain
20	chr2:51057200-51058800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:51057400-51057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:51057400-51058400	Weak transcription	Brain Anterior Caudate	brain
23	chr2:51057600-51058000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:51057600-51058800	Weak transcription	Fetal Brain Male	brain
25	chr2:51057800-51058200	Weak transcription	Fetal Brain Female	brain
26	chr2:51058000-51059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:51058200-51059800	Enhancers	Fetal Brain Female	brain
28	chr2:51058400-51058800	Enhancers	Brain Anterior Caudate	brain
29	chr2:51058400-51059800	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:51058600-51058800	Enhancers	Brain Hippocampus Middle	brain
31	chr2:51058600-51059400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr2:51058600-51059600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:51058600-51059800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr2:51058800-51059000	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr2:51058800-51059400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:51058800-51059400	Active TSS	Brain Anterior Caudate	brain
37	chr2:51058800-51060000	Enhancers	Fetal Brain Male	brain
38	chr2:51059000-51059200	Enhancers	Brain Hippocampus Middle	brain
39	chr2:51059200-51059400	Active TSS	Brain Hippocampus Middle	brain
40	chr2:51059400-51059800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:51059600-51065200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:51059800-51074200	Weak transcription	Brain Germinal Matrix	brain
43	chr2:51062000-51062200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr2:51062200-51063600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:51062200-51064400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr2:51063200-51063400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:51063400-51064600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:51063600-51063800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:51063800-51067800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:51064400-51064600	Enhancers	H1 Cell Line	embryonic stem cell

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