Variant report

Variant	nsv562136
Chromosome Location	chr13:67355618-67485147
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	ARID3A	chr13:67409290-67409647	K562	blood:	n/a	n/a
2	CBX3	chr13:67385534-67385881	K562	blood:	n/a	n/a
3	CCNT2	chr13:67480244-67480442	K562	blood:	n/a	n/a
4	CCNT2	chr13:67474239-67474501	K562	blood:	n/a	n/a
5	CCNT2	chr13:67368496-67368718	K562	blood:	n/a	n/a
6	CCNT2	chr13:67365175-67365485	K562	blood:	n/a	n/a
7	CEBPB	chr13:67379693-67380116	A549	lung:	n/a	chr13:67379983-67379994
8	CEBPB	chr13:67476147-67476615	H1-hESC	embryonic stem cell:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465
9	CEBPB	chr13:67484769-67485091	HepG2	liver:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
10	CEBPB	chr13:67484837-67485058	H1-hESC	embryonic stem cell:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
11	CEBPB	chr13:67484754-67485342	A549	lung:	n/a	chr13:67485279-67485292 chr13:67485279-67485290 chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
12	CEBPB	chr13:67484807-67485063	A549	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
13	CEBPB	chr13:67378268-67378811	Hela-S3	cervix:	n/a	chr13:67378729-67378740 chr13:67378729-67378740 chr13:67378544-67378557 chr13:67378441-67378458
14	CEBPB	chr13:67476335-67476625	HepG2	liver:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465
15	CEBPB	chr13:67394952-67395122	A549	lung:	n/a	n/a
16	CEBPB	chr13:67456481-67456509	IMR90	lung:	n/a	n/a
17	CEBPB	chr13:67484778-67485211	A549	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
18	CEBPB	chr13:67429391-67429576	A549	lung:	n/a	n/a
19	CEBPB	chr13:67484766-67485107	ECC-1	luminal epithelium:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
20	CEBPB	chr13:67374137-67374418	HepG2	liver:	n/a	chr13:67374286-67374297
21	CEBPB	chr13:67421612-67422123	A549	lung:	n/a	n/a
22	CEBPB	chr13:67379741-67380150	Hela-S3	cervix:	n/a	chr13:67379983-67379994
23	CEBPB	chr13:67394912-67395112	HepG2	liver:	n/a	n/a
24	CEBPB	chr13:67484755-67485097	IMR90	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
25	CEBPB	chr13:67484786-67485088	K562	blood:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
26	CEBPB	chr13:67476352-67476564	K562	blood:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465
27	CEBPB	chr13:67484840-67485040	Hela-S3	cervix:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
28	CEBPB	chr13:67421847-67422047	A549	lung:	n/a	n/a
29	CEBPB	chr13:67374231-67374333	H1-hESC	embryonic stem cell:	n/a	chr13:67374286-67374297
30	CTCF	chr13:67420981-67421059	LNCaP	prostate:	n/a	n/a
31	CTCF	chr13:67409240-67409390	GM12875	blood:	n/a	n/a
32	CTCF	chr13:67409600-67409750	HPF	lung:	n/a	n/a
33	CTCF	chr13:67409620-67409770	HEK293	kidney:	n/a	n/a
34	CTCF	chr13:67463855-67463909	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr13:67369382-67369431	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr13:67357180-67357330	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr13:67435100-67435250	GM12871	blood:	n/a	n/a
38	CTCF	chr13:67409340-67409490	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr13:67374100-67374250	HRE	kidney:	n/a	n/a
40	CTCF	chr13:67424096-67424113	HepG2	liver:	n/a	n/a
41	CTCF	chr13:67409600-67409750	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr13:67387060-67387210	NB4	blood:	n/a	n/a
43	CTCF	chr13:67409680-67409830	A549	lung:	n/a	n/a
44	CTCF	chr13:67374058-67374108	ProgFib	skin:	n/a	n/a
45	CTCF	chr13:67424040-67424190	GM12867	blood:	n/a	n/a
46	CTCF	chr13:67405780-67405930	HRE	kidney:	n/a	n/a
47	CTCF	chr13:67485091-67485162	Lung_OC	lung:	n/a	n/a
48	CTCF	chr13:67409620-67409770	BE2_C	brain:	n/a	n/a
49	CTCF	chr13:67394999-67395078	GM10248	blood:	n/a	n/a
50	CTCF	chr13:67409600-67409750	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67479146-67479196	AoSMC	blood vessel:	n/a
2	chr13:67478043-67478093	A549	lung:	n/a
3	chr13:67374653-67374703	Jurkat	blood:	n/a
4	chr13:67479146-67479196	AoSMC	blood vessel:	n/a
5	chr13:67478043-67478093	A549	lung:	n/a
6	chr13:67374653-67374703	Jurkat	blood:	n/a
7	chr13:67421996-67422046	A549	lung:	n/a
8	chr13:67478043-67478093	HAEpiC	amniotic membrane:	n/a
9	chr13:67478043-67478093	Jurkat	blood:	n/a
10	chr13:67434423-67434473	ECC-1	luminal epithelium:	n/a
11	chr13:67478043-67478093	AG09309	skin:	n/a
12	chr13:67374653-67374703	LNCaP	prostate:	n/a
13	chr13:67479146-67479196	HIPEpiC	eye:	n/a
14	chr13:67374653-67374703	HCF	heart:	n/a
15	chr13:67434423-67434473	HMEC	breast:	n/a
16	chr13:67374653-67374703	HIPEpiC	eye:	n/a
17	chr13:67479146-67479196	ovcar-3	ovarian:	n/a
18	chr13:67421996-67422046	HPAEpiC	pulmonary alveolar:	n/a
19	chr13:67434423-67434473	AG04450	lung:	fetal
20	chr13:67434423-67434473	U87	brain:	n/a
21	chr13:67434423-67434473	H1-hESC	embryonic stem cell:	embryo
22	chr13:67374653-67374703	HRPEpiC	eye:	n/a
23	chr13:67478043-67478093	BJ	skin:	n/a
24	chr13:67478043-67478093	H1-hESC	embryonic stem cell:	embryo
25	chr13:67374653-67374703	HPAEpiC	pulmonary alveolar:	n/a
26	chr13:67434423-67434473	NHBE	bronchial:	n/a
27	chr13:67374653-67374703	HRE	kidney:	n/a
28	chr13:67479146-67479196	IMR90	lung:	fetal
29	chr13:67478043-67478093	AG04450	lung:	fetal
30	chr13:67434423-67434473	HCPEpiC	choroid plexus:	n/a
31	chr13:67479146-67479196	RPTEC	kidney:	n/a
32	chr13:67421996-67422046	MCF-7	breast:	n/a
33	chr13:67479146-67479196	HCM	heart:	n/a
34	chr13:67374653-67374703	A549	lung:	n/a
35	chr13:67374653-67374703	HepG2	liver:	n/a
36	chr13:67434423-67434473	ovcar-3	ovarian:	n/a
37	chr13:67374653-67374703	T-47D	breast:	n/a
38	chr13:67374653-67374703	HAEpiC	amniotic membrane:	n/a
39	chr13:67374653-67374703	NH-A	brain:	n/a
40	chr13:67421996-67422046	NHDF-neo	bronchial:	n/a
41	chr13:67374653-67374703	SK-N-MC	brain:	n/a
42	chr13:67421996-67422046	HRE	kidney:	n/a
43	chr13:67374653-67374703	NHDF-neo	bronchial:	n/a
44	chr13:67374653-67374703	HUVEC	blood vessel:	n/a
45	chr13:67478043-67478093	GM19239	blood:	n/a
46	chr13:67478043-67478093	GM12891	blood:	n/a
47	chr13:67374653-67374703	BE2_C	brain:	n/a
48	chr13:67478043-67478093	HCF	heart:	n/a
49	chr13:67374653-67374703	AG10803	skin:	n/a
50	chr13:67479146-67479196	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:
2	chr13:67414851..67415422-chr7:70812042..70812870,2	MCF-7	breast:
3	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:
4	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
5	chr13:67397391..67400012-chr13:67432704..67434627,2	K562	blood:
6	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
7	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-14	chr13:67460132-67460209	ENSG00000228842.1
2	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.2
3	lnc-AL445989.1-14	chr13:67433120-67433252	ENSG00000228842.2
4	lnc-AL445989.1-14	chr13:67399301-67399368	ENSG00000228842.2
5	lnc-AL445989.1-14	chr13:67484006-67484154	NONHSAT034214
6	lnc-AL445989.1-14	chr13:67433130-67433252	ENSG00000228842.1
7	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.1
8	lnc-AL445989.1-14	chr13:67460132-67460208	ENSG00000228842.2

Variant related genes	Relation type
PCDH9-AS2	TF binding region
PCDH9-AS2	CpG island
ENSG00000228842	chromatin interactions

Extended variants
information (count: 3718 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3718 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs912192	chr13:67355618-67355619	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188644386	chr13:67355624-67355625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4591020	chr13:67355634-67355635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs571457298	chr13:67355660-67355661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191945829	chr13:67355662-67355663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78277472	chr13:67355707-67355708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576136419	chr13:67355733-67355734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368315898	chr13:67355808-67355809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535764844	chr13:67355829-67355830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144331738	chr13:67355839-67355840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572015832	chr13:67355847-67355848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552768497	chr13:67355854-67355855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557783481	chr13:67355872-67355873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9540911	chr13:67355886-67355887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs543525884	chr13:67355913-67355914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377242087	chr13:67355918-67355919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563932927	chr13:67355922-67355923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148772307	chr13:67355938-67355939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376623076	chr13:67355943-67355944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35254607	chr13:67356018-67356019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67858833	chr13:67356019-67356020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3042287	chr13:67356021-67356022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111878576	chr13:67356022-67356023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183704887	chr13:67356058-67356059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559751359	chr13:67356067-67356068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9540912	chr13:67356095-67356096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34936581	chr13:67356151-67356152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142431035	chr13:67356158-67356159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551405633	chr13:67356160-67356161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113523162	chr13:67356162-67356163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530939942	chr13:67356192-67356193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550770861	chr13:67356193-67356194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139003814	chr13:67356321-67356322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535253969	chr13:67356333-67356334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74093604	chr13:67356347-67356348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs373785623	chr13:67356368-67356369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77856437	chr13:67356483-67356484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557818231	chr13:67356511-67356512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569149773	chr13:67356575-67356576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9564350	chr13:67356584-67356585	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs556745238	chr13:67356592-67356593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377492158	chr13:67356666-67356667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574182126	chr13:67356675-67356676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554681579	chr13:67356704-67356705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542902030	chr13:67356729-67356730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7994100	chr13:67356731-67356732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534038255	chr13:67356736-67356737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528797017	chr13:67356737-67356738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9540913	chr13:67356751-67356752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs564960627	chr13:67356752-67356753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67346200-67368400	Weak transcription	Brain Hippocampus Middle	brain
2	chr13:67354400-67355800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:67354600-67355800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:67354800-67355800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr13:67355200-67356600	Weak transcription	Fetal Brain Female	brain
6	chr13:67355400-67355800	Enhancers	HSMMtube	muscle
7	chr13:67355600-67374000	Weak transcription	HSMM	muscle
8	chr13:67355800-67357000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr13:67356800-67357000	Enhancers	Fetal Brain Female	brain
10	chr13:67357200-67357400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr13:67357200-67357600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:67362400-67364200	Enhancers	Brain Substantia Nigra	brain
13	chr13:67362600-67363400	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr13:67363000-67363200	Enhancers	Brain Cingulate Gyrus	brain
15	chr13:67363200-67363600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr13:67363200-67369600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr13:67364200-67368400	Weak transcription	Brain Substantia Nigra	brain
18	chr13:67365000-67365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:67367600-67368200	Enhancers	Primary B cells from cord blood	blood
20	chr13:67368200-67368400	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr13:67368400-67368600	Enhancers	Primary B cells from cord blood	blood
22	chr13:67368400-67368600	Enhancers	Brain Substantia Nigra	brain
23	chr13:67368400-67368800	Enhancers	Brain Hippocampus Middle	brain
24	chr13:67368400-67369200	Enhancers	Primary B cells from peripheral blood	blood
25	chr13:67368400-67369200	Enhancers	Fetal Brain Male	brain
26	chr13:67368600-67368800	Flanking Active TSS	Brain Substantia Nigra	brain
27	chr13:67368600-67369000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:67368600-67369000	Enhancers	Brain Angular Gyrus	brain
29	chr13:67368600-67369000	Enhancers	Brain Anterior Caudate	brain
30	chr13:67368600-67369200	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr13:67368800-67369200	Enhancers	Brain Substantia Nigra	brain
32	chr13:67368800-67369800	Weak transcription	Brain Hippocampus Middle	brain
33	chr13:67369000-67370000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:67369000-67370000	Weak transcription	Brain Angular Gyrus	brain
35	chr13:67369000-67370000	Weak transcription	Brain Anterior Caudate	brain
36	chr13:67369200-67369600	Enhancers	Primary B cells from cord blood	blood
37	chr13:67369200-67369800	Weak transcription	Brain Substantia Nigra	brain
38	chr13:67369200-67370200	Weak transcription	Fetal Brain Male	brain
39	chr13:67369600-67370000	Enhancers	Brain Cingulate Gyrus	brain
40	chr13:67369800-67370000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr13:67369800-67370000	Enhancers	Brain Substantia Nigra	brain
42	chr13:67369800-67370400	Active TSS	Brain Hippocampus Middle	brain
43	chr13:67370000-67370200	Active TSS	Brain Anterior Caudate	brain
44	chr13:67370000-67370400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:67370000-67370400	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr13:67370000-67370600	Flanking Active TSS	Brain Cingulate Gyrus	brain
47	chr13:67370000-67370600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr13:67370000-67370800	Enhancers	Brain Angular Gyrus	brain
49	chr13:67370000-67370800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr13:67370200-67370400	Flanking Active TSS	Brain Anterior Caudate	brain

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