Variant report

Variant	esv1843472
Chromosome Location	chr1:145171723-145258234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1740)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1740 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
2	ARID3A	chr1:145208951-145209121	K562	blood:	n/a	chr1:145209007-145209015
3	ARID3A	chr1:145208929-145209290	HepG2	liver:	n/a	chr1:145209007-145209015
4	ARID3A	chr1:145246167-145246562	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:145253698-145253898	K562	blood:	n/a	n/a
6	ATF1	chr1:145195978-145196042	K562	blood:	n/a	n/a
7	ATF1	chr1:145208937-145209133	K562	blood:	n/a	n/a
8	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
9	ATF1	chr1:145216140-145216326	K562	blood:	n/a	n/a
10	ATF2	chr1:145208822-145209212	GM12878	blood:	n/a	n/a
11	ATF2	chr1:145233655-145233883	GM12878	blood:	n/a	n/a
12	ATF3	chr1:145208814-145209112	A549	lung:	n/a	n/a
13	ATF3	chr1:145208827-145209217	A549	lung:	n/a	n/a
14	BACH1	chr1:145208936-145209146	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
16	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
18	BATF	chr1:145219743-145220000	GM12878	blood:	n/a	n/a
19	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
20	BATF	chr1:145210057-145210394	GM12878	blood:	n/a	n/a
21	BATF	chr1:145171479-145171789	GM12878	blood:	n/a	n/a
22	BATF	chr1:145233237-145234045	GM12878	blood:	n/a	n/a
23	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
24	BATF	chr1:145208490-145209291	GM12878	blood:	n/a	chr1:145209134-145209142
25	BATF	chr1:145231709-145232035	GM12878	blood:	n/a	n/a
26	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
27	BATF	chr1:145212001-145212472	GM12878	blood:	n/a	n/a
28	BATF	chr1:145189103-145189407	GM12878	blood:	n/a	n/a
29	BATF	chr1:145212132-145212476	GM12878	blood:	n/a	n/a
30	BATF	chr1:145213599-145213876	GM12878	blood:	n/a	n/a
31	BATF	chr1:145218967-145219192	GM12878	blood:	n/a	chr1:145218977-145218990
32	BATF	chr1:145209382-145209998	GM12878	blood:	n/a	n/a
33	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
34	BATF	chr1:145210075-145210284	GM12878	blood:	n/a	n/a
35	BATF	chr1:145195914-145196301	GM12878	blood:	n/a	n/a
36	BATF	chr1:145210338-145210530	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:145234917-145235601	GM12878	blood:	n/a	chr1:145235133-145235142
38	BCL11A	chr1:145233623-145234034	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:145226112-145226390	GM12878	blood:	n/a	chr1:145226287-145226296
40	BCL11A	chr1:145212041-145212491	GM12878	blood:	n/a	n/a
41	BCL11A	chr1:145228759-145228989	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:145233149-145234028	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:145227104-145227285	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:145195841-145196148	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:145253572-145253790	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:145211543-145211917	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:145208542-145209895	GM12878	blood:	n/a	chr1:145209027-145209040 chr1:145209689-145209702 chr1:145209045-145209058 chr1:145209538-145209551 chr1:145209041-145209054 chr1:145209454-145209462 chr1:145209010-145209019
48	BCL11A	chr1:145208600-145209261	GM12878	blood:	n/a	chr1:145209027-145209040 chr1:145209045-145209058 chr1:145209041-145209054 chr1:145209010-145209019
49	BCL11A	chr1:145233236-145233532	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:145234388-145234726	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145205174-145205224	GM12878	blood:	n/a
2	chr1:145211389-145211439	HRCEpiC	kidney:	n/a
3	chr1:145207943-145207993	HNPCEpiC	eye:	n/a
4	chr1:145250914-145250964	HIPEpiC	eye:	n/a
5	chr1:145205174-145205224	MCF10A-Er-Src	breast:	n/a
6	chr1:145210014-145210064	PrEC	prostate:	n/a
7	chr1:145209930-145209980	PrEC	prostate:	n/a
8	chr1:145207943-145207993	HUVEC	blood vessel:	n/a
9	chr1:145250914-145250964	HCT-116	colon:	n/a
10	chr1:145250914-145250964	K562	blood:	n/a
11	chr1:145208980-145209030	GM12891	blood:	n/a
12	chr1:145207943-145207993	NH-A	brain:	n/a
13	chr1:145211389-145211439	MCF10A-Er-Src	breast:	n/a
14	chr1:145207943-145207993	SK-N-MC	brain:	n/a
15	chr1:145211389-145211439	AG04449	skin:	fetal
16	chr1:145250914-145250964	AG04449	skin:	fetal
17	chr1:145208980-145209030	ECC-1	luminal epithelium:	n/a
18	chr1:145250914-145250964	NHDF-neo	bronchial:	n/a
19	chr1:145209236-145209286	A549	lung:	n/a
20	chr1:145213338-145213388	HUVEC	blood vessel:	n/a
21	chr1:145208980-145209030	PANC-1	pancreas:	n/a
22	chr1:145208980-145209030	SAEC	small airway:	n/a
23	chr1:145213338-145213388	Hepatocyte	liver:	n/a
24	chr1:145209236-145209286	NHBE	bronchial:	n/a
25	chr1:145207943-145207993	PFSK-1	brain:	n/a
26	chr1:145208980-145209030	HCT-116	colon:	n/a
27	chr1:145211389-145211439	CMK	blood:	n/a
28	chr1:145210014-145210064	AG09309	skin:	n/a
29	chr1:145213338-145213388	HCM	heart:	n/a
30	chr1:145209930-145209980	Hela-S3	cervix:	n/a
31	chr1:145210014-145210064	HRCEpiC	kidney:	n/a
32	chr1:145213338-145213388	NHBE	bronchial:	n/a
33	chr1:145209930-145209980	HNPCEpiC	eye:	n/a
34	chr1:145250914-145250964	BJ	skin:	n/a
35	chr1:145209930-145209980	SK-N-SH	brain:	n/a
36	chr1:145209236-145209286	HUVEC	blood vessel:	n/a
37	chr1:145205174-145205224	HEK293	kidney:	embryo
38	chr1:145209236-145209286	RPTEC	kidney:	n/a
39	chr1:145209930-145209980	HCF	heart:	n/a
40	chr1:145208980-145209030	HEEpiC	esophagus:	n/a
41	chr1:145250914-145250964	PANC-1	pancreas:	n/a
42	chr1:145250914-145250964	Caco-2	colon:	n/a
43	chr1:145209830-145209880	AG04450	lung:	fetal
44	chr1:145208980-145209030	AoSMC	blood vessel:	n/a
45	chr1:145213338-145213388	NB4	blood:	n/a
46	chr1:145209930-145209980	HUVEC	blood vessel:	n/a
47	chr1:145210014-145210064	HepG2	liver:	n/a
48	chr1:145209236-145209286	LNCaP	prostate:	n/a
49	chr1:145211389-145211439	NB4	blood:	n/a
50	chr1:145250914-145250964	SKMC	muscle:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120561821..120563990-chr1:145256491..145258504,4	MCF-7	breast:
2	chr1:120576520..120578439-chr1:145242059..145244929,2	MCF-7	breast:
3	chr1:120602747..120604407-chr1:145216153..145218112,2	MCF-7	breast:
4	chr1:120611958..120612515-chr1:145208972..145209639,2	NB4	blood:
5	chr1:53163301..53163992-chr1:145209547..145210339,2	Hela-S3	cervix:
6	chr1:145208214..145210170-chr1:145381446..145384467,3	MCF-7	breast:
7	chr1:120610094..120613669-chr1:145207447..145211087,11	MCF-7	breast:
8	chr1:120606120..120607638-chr1:145207438..145208952,2	MCF-7	breast:
9	chr1:145210633..145213326-chr1:149222498..149224954,2	MCF-7	breast:
10	chr1:120562393..120564845-chr1:145256114..145258582,3	MCF-7	breast:
11	chr1:120562041..120564945-chr1:145257130..145258905,2	K562	blood:
12	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
13	chr1:145209435..145210070-chr1:145293272..145293941,2	MCF-7	breast:
14	chr1:145193254..145195284-chr1:145382712..145384267,2	MCF-7	breast:
15	chr1:145209931..145210445-chr19:58874333..58874839,2	Hela-S3	cervix:
16	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
17	chr1:120610124..120613523-chr1:145208226..145211226,7	MCF-7	breast:
18	chr1:145246366..145248846-chr1:149222454..149225152,2	MCF-7	breast:
19	chr1:120611803..120612535-chr1:145208972..145209627,6	MCF-7	breast:
20	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
21	chr1:120573750..120576750-chr1:145244417..145247281,4	MCF-7	breast:
22	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
23	chr1:145209779..145211659-chr1:145381647..145384503,2	MCF-7	breast:
24	chr1:120565033..120566748-chr1:145252742..145255259,2	MCF-7	breast:
25	chr1:120611941..120612674-chr1:145209107..145209637,6	MCF-7	breast:
26	chr1:145209133..145210911-chr1:145213297..145216185,2	MCF-7	breast:
27	chr1:120611825..120612753-chr1:145208933..145209629,3	Hela-S3	cervix:
28	chr1:145207909..145210605-chr1:145214441..145216644,2	MCF-7	breast:
29	chr1:120574754..120575346-chr1:145245858..145246575,2	MCF-7	breast:
30	chr1:145209043..145210611-chr1:149222292..149224968,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBPF10-1	chr1:145213108-145213374	expReg_chr1_15650_+
2	lnc-PDE4DIP-6	chr1:145200338-145200891	ENSG00000272709.1

No data

Variant related genes	Relation type
ENSG00000272709	TF binding region
NOTCH2NL	TF binding region
ENSG00000255168	TF binding region
ENSG00000272709	CpG island
NOTCH2NL	CpG island
ENSG00000255168	CpG island
ENSG00000163386	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000213240	chromatin interactions
ENSG00000162377	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000252211	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000201558	chromatin interactions

Extended variants
information (count: 2351 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2351 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587707591	chr1:145171764-145171765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150633344	chr1:145171772-145171773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587606149	chr1:145171800-145171801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115223778	chr1:145171863-145171864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587680608	chr1:145171866-145171867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587764199	chr1:145171870-145171871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587737651	chr1:145171880-145171881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78874790	chr1:145171893-145171894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587594575	chr1:145171952-145171953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587695053	chr1:145171979-145171980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587731019	chr1:145172022-145172023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587620880	chr1:145172039-145172040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587660878	chr1:145172083-145172084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367857298	chr1:145172086-145172087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587729945	chr1:145172107-145172108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587631967	chr1:145172127-145172128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372208148	chr1:145172182-145172183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587767744	chr1:145172220-145172221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6424341	chr1:145172238-145172239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587703879	chr1:145172287-145172288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2603831	chr1:145172330-145172331	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs587757500	chr1:145172373-145172374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587649405	chr1:145172385-145172386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587706433	chr1:145172405-145172406	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374209240	chr1:145172407-145172408	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs587756907	chr1:145172410-145172411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs587657882	chr1:145172504-145172505	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377187553	chr1:145172512-145172513	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs587735998	chr1:145172529-145172530	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587615341	chr1:145172566-145172567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs200345714	chr1:145172606-145172607	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs4649811	chr1:145172618-145172619	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs201628056	chr1:145172647-145172648	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs587694988	chr1:145172721-145172722	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs587701724	chr1:145172772-145172773	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587607358	chr1:145172774-145172775	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs587671780	chr1:145172883-145172884	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs140771561	chr1:145172901-145172902	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs587733328	chr1:145172932-145172933	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs587632348	chr1:145172989-145172990	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587665260	chr1:145173020-145173021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587749336	chr1:145173055-145173056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202172867	chr1:145173058-145173059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587624265	chr1:145173384-145173385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587700481	chr1:145173398-145173399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587723924	chr1:145173414-145173415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587625977	chr1:145173547-145173548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369431261	chr1:145173632-145173633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587759422	chr1:145173641-145173642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587660338	chr1:145173780-145173781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	20808228	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145160200-145178000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:145164400-145175400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:145170800-145173200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:145170800-145174000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr1:145170800-145176000	Enhancers	Primary B cells from cord blood	blood
6	chr1:145170800-145176400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:145171000-145171800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:145171000-145172000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:145171000-145172000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:145171000-145172000	Enhancers	GM12878-XiMat	blood
11	chr1:145171000-145174400	Enhancers	Primary B cells from peripheral blood	blood
12	chr1:145171200-145176200	Weak transcription	Spleen	Spleen
13	chr1:145171400-145172400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:145171600-145176000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:145171800-145172600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:145172000-145174400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:145172000-145176200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:145172000-145177400	Weak transcription	GM12878-XiMat	blood
19	chr1:145172400-145173000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr1:145172600-145172800	Enhancers	Esophagus	oesophagus
21	chr1:145172600-145172800	Enhancers	HMEC	breast
22	chr1:145172600-145173400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:145172600-145173400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:145172800-145173800	Weak transcription	Esophagus	oesophagus
25	chr1:145173000-145175400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:145173200-145173600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:145173400-145173600	Enhancers	HMEC	breast
28	chr1:145173400-145176200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:145173600-145176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:145173800-145174000	Enhancers	Fetal Lung	lung
31	chr1:145173800-145174200	Enhancers	Esophagus	oesophagus
32	chr1:145174000-145175400	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr1:145174400-145174800	Weak transcription	Primary B cells from peripheral blood	blood
34	chr1:145174400-145176600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:145174800-145176200	Enhancers	Primary B cells from peripheral blood	blood
36	chr1:145175000-145176600	Enhancers	K562	blood
37	chr1:145175400-145175600	Enhancers	Fetal Lung	lung
38	chr1:145175400-145176400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr1:145175400-145176600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr1:145175400-145178000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr1:145176000-145176200	Flanking Active TSS	Primary B cells from cord blood	blood
42	chr1:145176000-145176200	Enhancers	Primary T cells from cord blood	blood
43	chr1:145176000-145176200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr1:145176000-145176200	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr1:145176000-145176600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:145176000-145177400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr1:145176000-145177600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:145176000-145178200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr1:145176000-145178200	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr1:145176000-145178800	Enhancers	Primary T helper cells PMA-I stimulated	--

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