Variant report

Variant	nsv931853
Chromosome Location	chr2:51066578-51260667
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	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
12	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
13	CEBPB	chr2:51185052-51185376	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
14	CEBPB	chr2:51256083-51256253	HepG2	liver:	n/a	chr2:51256172-51256183
15	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
17	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
18	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
19	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
20	CEBPB	chr2:51185039-51185390	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
21	CEBPB	chr2:51229690-51229927	A549	lung:	n/a	chr2:51229820-51229831
22	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
23	CEBPB	chr2:51256005-51256373	Hela-S3	cervix:	n/a	chr2:51256172-51256183
24	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
25	CEBPB	chr2:51180217-51180418	K562	blood:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
26	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
28	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
29	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
30	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
32	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
34	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
35	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
36	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
37	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
38	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
39	CEBPB	chr2:51185014-51185411	Hela-S3	cervix:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
40	CEBPB	chr2:51179698-51180729	Hela-S3	cervix:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
41	CEBPB	chr2:51179722-51180770	HCT-116	colon:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
42	CEBPB	chr2:51185053-51185350	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
43	CEBPB	chr2:51184010-51184263	HepG2	liver:	n/a	chr2:51184131-51184142
44	CEBPB	chr2:51229679-51229969	HepG2	liver:	n/a	chr2:51229820-51229831
45	CEBPB	chr2:51255998-51256347	A549	lung:	n/a	chr2:51256172-51256183
46	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
48	CEBPB	chr2:51180165-51180469	A549	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
49	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
50	CEBPB	chr2:51185005-51185419	IMR90	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51260003-51260053	SAEC	small airway:	n/a
2	chr2:51254170-51254220	AG04449	skin:	fetal
3	chr2:51228125-51228175	Hepatocyte	liver:	n/a
4	chr2:51260003-51260053	SAEC	small airway:	n/a
5	chr2:51254170-51254220	AG04449	skin:	fetal
6	chr2:51228125-51228175	Hepatocyte	liver:	n/a
7	chr2:51259807-51259857	NT2-D1	testis:	n/a
8	chr2:51254132-51254182	ProgFib	skin:	n/a
9	chr2:51074939-51074989	SK-N-SH	brain:	n/a
10	chr2:51254132-51254182	NHBE	bronchial:	n/a
11	chr2:51259493-51259543	NHBE	bronchial:	n/a
12	chr2:51254021-51254071	HCF	heart:	n/a
13	chr2:51228125-51228175	AG04449	skin:	fetal
14	chr2:51254021-51254071	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:51228125-51228175	NHBE	bronchial:	n/a
16	chr2:51240310-51240360	AG09319	gingival:	n/a
17	chr2:51255324-51255374	SKMC	muscle:	n/a
18	chr2:51259807-51259857	MCF-7	breast:	n/a
19	chr2:51254170-51254220	Hela-S3	cervix:	n/a
20	chr2:51259693-51259743	HCPEpiC	choroid plexus:	n/a
21	chr2:51254132-51254182	HL-60	blood:	n/a
22	chr2:51254102-51254152	HNPCEpiC	eye:	n/a
23	chr2:51254981-51255031	GM12892	blood:	n/a
24	chr2:51259786-51259836	HCPEpiC	choroid plexus:	n/a
25	chr2:51228125-51228175	SAEC	small airway:	n/a
26	chr2:51259552-51259602	HEK293	kidney:	embryo
27	chr2:51255324-51255374	LNCaP	prostate:	n/a
28	chr2:51228125-51228175	HAEpiC	amniotic membrane:	n/a
29	chr2:51254823-51254873	Hela-S3	cervix:	n/a
30	chr2:51252301-51252351	GM12892	blood:	n/a
31	chr2:51252301-51252351	ovcar-3	ovarian:	n/a
32	chr2:51254170-51254220	K562	blood:	n/a
33	chr2:51259703-51259753	SK-N-SH	brain:	n/a
34	chr2:51252301-51252351	Caco-2	colon:	n/a
35	chr2:51259493-51259543	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:51252301-51252351	HAEpiC	amniotic membrane:	n/a
37	chr2:51260399-51260449	MCF-7	breast:	n/a
38	chr2:51254170-51254220	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:51254823-51254873	HEEpiC	esophagus:	n/a
40	chr2:51259693-51259743	NHDF-neo	bronchial:	n/a
41	chr2:51259552-51259602	AG10803	skin:	n/a
42	chr2:51259703-51259753	Hela-S3	cervix:	n/a
43	chr2:51259493-51259543	PFSK-1	brain:	n/a
44	chr2:51254021-51254071	Hela-S3	cervix:	n/a
45	chr2:51255627-51255677	ProgFib	skin:	n/a
46	chr2:51260399-51260449	SK-N-MC	brain:	n/a
47	chr2:51231649-51231699	HAEpiC	amniotic membrane:	n/a
48	chr2:51259807-51259857	A549	lung:	n/a
49	chr2:51074939-51074989	BE2_C	brain:	n/a
50	chr2:51255627-51255677	LNCaP	prostate:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1

Variant related genes	Relation type
ENSG00000231918	TF binding region
NRXN1	TF binding region
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region
ENSG00000231918	CpG island
NRXN1	CpG island
ENSG00000216011	CpG island
ENSG00000272385	CpG island

Extended variants
information (count: 7841 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:7841 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572334747	chr2:51066634-51066635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571089806	chr2:51066681-51066682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79444154	chr2:51066687-51066688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367701906	chr2:51066704-51066705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556332121	chr2:51066717-51066718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577864858	chr2:51066720-51066721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193220186	chr2:51066771-51066772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184446499	chr2:51066788-51066789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572373821	chr2:51066798-51066799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542658926	chr2:51066805-51066806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540966316	chr2:51066833-51066834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561391933	chr2:51066834-51066835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs68157830	chr2:51066869-51066870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs189580778	chr2:51066875-51066876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144840636	chr2:51066925-51066926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532383381	chr2:51066927-51066928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547681015	chr2:51066938-51066939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148578108	chr2:51066960-51066961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574844878	chr2:51067017-51067018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180809916	chr2:51067260-51067261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141157765	chr2:51067280-51067281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs759541	chr2:51067290-51067291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557858424	chr2:51067332-51067333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536748548	chr2:51067421-51067422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551886002	chr2:51067428-51067429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563747707	chr2:51067497-51067498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571658781	chr2:51067504-51067505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571471612	chr2:51067530-51067531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538866354	chr2:51067531-51067532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534012065	chr2:51067551-51067552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185639357	chr2:51067559-51067560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373924762	chr2:51067585-51067586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188352398	chr2:51067605-51067606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181571780	chr2:51067658-51067659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11675267	chr2:51067675-51067676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs576533497	chr2:51067764-51067765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371219788	chr2:51067769-51067770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543920047	chr2:51067782-51067783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565395677	chr2:51067807-51067808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185718532	chr2:51067808-51067809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111829794	chr2:51067846-51067847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72838714	chr2:51067860-51067861	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559561436	chr2:51067866-51067867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376993004	chr2:51067891-51067892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192026159	chr2:51067893-51067894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10490176	chr2:51067934-51067935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528826041	chr2:51067941-51067942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563117030	chr2:51068004-51068005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530438029	chr2:51068014-51068015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551825308	chr2:51068024-51068025	Weak transcription Enhancers	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51059800-51074200	Weak transcription	Brain Germinal Matrix	brain
2	chr2:51063800-51067800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:51066000-51067600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:51066000-51074600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:51066200-51067400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:51066200-51067600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:51066200-51073000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:51067600-51067800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:51067600-51068000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:51067600-51068200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:51067800-51068400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:51068000-51068400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr2:51068400-51069200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:51069200-51070000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr2:51070000-51078000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:51071200-51076000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:51073000-51073600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:51073200-51074400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:51073400-51073600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr2:51073400-51073600	Enhancers	Ovary	ovary
21	chr2:51073400-51074400	Enhancers	Fetal Kidney	kidney
22	chr2:51073600-51074200	Weak transcription	Ovary	ovary
23	chr2:51074200-51074400	Enhancers	Brain Germinal Matrix	brain
24	chr2:51074200-51075000	Enhancers	Ovary	ovary
25	chr2:51074400-51076200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:51074400-51076800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:51074600-51075000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:51074800-51075000	Enhancers	Pancreas	Pancrea
29	chr2:51075000-51084400	Weak transcription	Ovary	ovary
30	chr2:51075200-51077200	Weak transcription	Pancreas	Pancrea
31	chr2:51076800-51077000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:51077000-51077400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:51077200-51077400	Enhancers	Pancreas	Pancrea
34	chr2:51077200-51077800	Enhancers	Liver	Liver
35	chr2:51077200-51078200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:51077400-51078200	Weak transcription	Pancreas	Pancrea
37	chr2:51077400-51078400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:51077600-51078600	Enhancers	Fetal Brain Male	brain
39	chr2:51078000-51078200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr2:51078200-51078400	Enhancers	Fetal Brain Female	brain
41	chr2:51078200-51078800	Enhancers	Pancreas	Pancrea
42	chr2:51078200-51089600	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:51078400-51079200	Weak transcription	Fetal Brain Female	brain
44	chr2:51078600-51079000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:51078600-51080200	Weak transcription	Fetal Brain Male	brain
46	chr2:51079200-51079400	Enhancers	Fetal Brain Female	brain
47	chr2:51079400-51080200	Weak transcription	Fetal Brain Female	brain
48	chr2:51080000-51080400	Enhancers	Brain Germinal Matrix	brain
49	chr2:51080200-51080600	Enhancers	Fetal Brain Male	brain
50	chr2:51080200-51080800	Enhancers	Fetal Brain Female	brain

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