Variant report

Variant	nsv430580
Chromosome Location	chr13:67352439-67468100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

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	chr13:67368496-67368718	K562	blood:	n/a	n/a
4	CCNT2	chr13:67365175-67365485	K562	blood:	n/a	n/a
5	CEBPB	chr13:67456481-67456509	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:67374137-67374418	HepG2	liver:	n/a	chr13:67374286-67374297
7	CEBPB	chr13:67355095-67355295	A549	lung:	n/a	n/a
8	CEBPB	chr13:67374231-67374333	H1-hESC	embryonic stem cell:	n/a	chr13:67374286-67374297
9	CEBPB	chr13:67355027-67355238	IMR90	lung:	n/a	n/a
10	CEBPB	chr13:67378268-67378811	Hela-S3	cervix:	n/a	chr13:67378729-67378740 chr13:67378729-67378740 chr13:67378544-67378557 chr13:67378441-67378458
11	CEBPB	chr13:67421847-67422047	A549	lung:	n/a	n/a
12	CEBPB	chr13:67354973-67355302	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr13:67394912-67395112	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:67379693-67380116	A549	lung:	n/a	chr13:67379983-67379994
15	CEBPB	chr13:67352565-67352886	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:67352566-67352866	IMR90	lung:	n/a	n/a
17	CEBPB	chr13:67429391-67429576	A549	lung:	n/a	n/a
18	CEBPB	chr13:67379741-67380150	Hela-S3	cervix:	n/a	chr13:67379983-67379994
19	CEBPB	chr13:67421612-67422123	A549	lung:	n/a	n/a
20	CEBPB	chr13:67352551-67352852	A549	lung:	n/a	n/a
21	CEBPB	chr13:67394952-67395122	A549	lung:	n/a	n/a
22	CTCF	chr13:67387060-67387210	NB4	blood:	n/a	n/a
23	CTCF	chr13:67374058-67374108	ProgFib	skin:	n/a	n/a
24	CTCF	chr13:67435100-67435250	GM12871	blood:	n/a	n/a
25	CTCF	chr13:67409600-67409750	BE2_C	brain:	n/a	n/a
26	CTCF	chr13:67409600-67409750	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr13:67409340-67409490	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr13:67424040-67424190	GM12867	blood:	n/a	n/a
29	CTCF	chr13:67409620-67409770	BE2_C	brain:	n/a	n/a
30	CTCF	chr13:67409600-67409750	HPF	lung:	n/a	n/a
31	CTCF	chr13:67424096-67424113	HepG2	liver:	n/a	n/a
32	CTCF	chr13:67409240-67409390	GM12875	blood:	n/a	n/a
33	CTCF	chr13:67394999-67395078	GM10248	blood:	n/a	n/a
34	CTCF	chr13:67463855-67463909	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr13:67357180-67357330	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr13:67409300-67409450	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr13:67420981-67421059	LNCaP	prostate:	n/a	n/a
38	CTCF	chr13:67409620-67409770	HEK293	kidney:	n/a	n/a
39	CTCF	chr13:67369382-67369431	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr13:67409680-67409830	A549	lung:	n/a	n/a
41	CTCF	chr13:67374100-67374250	HRE	kidney:	n/a	n/a
42	CTCF	chr13:67405780-67405930	HRE	kidney:	n/a	n/a
43	CUX1	chr13:67438613-67438637	K562	blood:	n/a	n/a
44	CUX1	chr13:67420153-67420166	K562	blood:	n/a	n/a
45	E2F4	chr13:67364844-67365015	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr13:67403495-67403634	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr13:67404479-67404547	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:67355029-67355298	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:67410109-67410314	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr13:67432774-67432869	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67434423-67434473	HRCEpiC	kidney:	n/a
2	chr13:67421996-67422046	BE2_C	brain:	n/a
3	chr13:67374653-67374703	HRCEpiC	kidney:	n/a
4	chr13:67374653-67374703	HRPEpiC	eye:	n/a
5	chr13:67374653-67374703	HRE	kidney:	n/a
6	chr13:67421996-67422046	T-47D	breast:	n/a
7	chr13:67421996-67422046	HRCEpiC	kidney:	n/a
8	chr13:67374653-67374703	ProgFib	skin:	n/a
9	chr13:67374653-67374703	AG09319	gingival:	n/a
10	chr13:67421996-67422046	NT2-D1	testis:	n/a
11	chr13:67434423-67434473	HIPEpiC	eye:	n/a
12	chr13:67434423-67434473	HAEpiC	amniotic membrane:	n/a
13	chr13:67434423-67434473	Jurkat	blood:	n/a
14	chr13:67374653-67374703	AG04450	lung:	fetal
15	chr13:67434423-67434473	K562	blood:	n/a
16	chr13:67374653-67374703	LNCaP	prostate:	n/a
17	chr13:67421996-67422046	SKMC	muscle:	n/a
18	chr13:67421996-67422046	GM12892	blood:	n/a
19	chr13:67421996-67422046	HCPEpiC	choroid plexus:	n/a
20	chr13:67421996-67422046	AG04449	skin:	fetal
21	chr13:67374653-67374703	GM12878	blood:	n/a
22	chr13:67374653-67374703	GM12891	blood:	n/a
23	chr13:67434423-67434473	AG04450	lung:	fetal
24	chr13:67434423-67434473	MCF10A-Er-Src	breast:	n/a
25	chr13:67434423-67434473	SAEC	small airway:	n/a
26	chr13:67421996-67422046	NHDF-neo	bronchial:	n/a
27	chr13:67421996-67422046	H1-hESC	embryonic stem cell:	embryo
28	chr13:67374653-67374703	AoSMC	blood vessel:	n/a
29	chr13:67374653-67374703	SKMC	muscle:	n/a
30	chr13:67421996-67422046	RPTEC	kidney:	n/a
31	chr13:67374653-67374703	Caco-2	colon:	n/a
32	chr13:67374653-67374703	Jurkat	blood:	n/a
33	chr13:67421996-67422046	GM12878	blood:	n/a
34	chr13:67421996-67422046	HepG2	liver:	n/a
35	chr13:67434423-67434473	HCT-116	colon:	n/a
36	chr13:67374653-67374703	SK-N-SH_RA	brain:	n/a
37	chr13:67434423-67434473	PANC-1	pancreas:	n/a
38	chr13:67374653-67374703	SK-N-SH	brain:	n/a
39	chr13:67434423-67434473	NHDF-neo	bronchial:	n/a
40	chr13:67374653-67374703	NB4	blood:	n/a
41	chr13:67434423-67434473	H1-hESC	embryonic stem cell:	embryo
42	chr13:67421996-67422046	AG04450	lung:	fetal
43	chr13:67421996-67422046	HCT-116	colon:	n/a
44	chr13:67374653-67374703	AG04449	skin:	fetal
45	chr13:67374653-67374703	HL-60	blood:	n/a
46	chr13:67434423-67434473	GM12891	blood:	n/a
47	chr13:67421996-67422046	SK-N-MC	brain:	n/a
48	chr13:67434423-67434473	IMR90	lung:	fetal
49	chr13:67434423-67434473	AG09319	gingival:	n/a
50	chr13:67434423-67434473	HL-60	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:67455570..67458044-chr13:67459396..67461929,2	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	chr13:67397391..67400012-chr13:67432704..67434627,2	K562	blood:
5	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
6	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3210 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3210 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2324988	chr13:67352439-67352440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139986379	chr13:67352482-67352483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554415332	chr13:67352500-67352501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74482761	chr13:67352509-67352510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555857514	chr13:67352584-67352585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2324989	chr13:67352587-67352588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576651248	chr13:67352608-67352609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2875502	chr13:67352645-67352646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs530385808	chr13:67352749-67352750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116313303	chr13:67352788-67352789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553973450	chr13:67352801-67352802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540173287	chr13:67352818-67352819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560354791	chr13:67352834-67352835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531981677	chr13:67352918-67352919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551800523	chr13:67352973-67352974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568502164	chr13:67352981-67352982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531338053	chr13:67352983-67352984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548710462	chr13:67353048-67353049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111668895	chr13:67353080-67353081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548242523	chr13:67353091-67353092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9564349	chr13:67353206-67353207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534365830	chr13:67353233-67353234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554175283	chr13:67353274-67353275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185302477	chr13:67353286-67353287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368685061	chr13:67353325-67353326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565024402	chr13:67353342-67353343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73210276	chr13:67353357-67353358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557752793	chr13:67353526-67353527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576484290	chr13:67353550-67353551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145440525	chr13:67353568-67353569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77190570	chr13:67353585-67353586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7322333	chr13:67353608-67353609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555796058	chr13:67353622-67353623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574555631	chr13:67353628-67353629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148825556	chr13:67353633-67353634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559909015	chr13:67353681-67353682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532311692	chr13:67353682-67353683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113252150	chr13:67353683-67353684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146457820	chr13:67353745-67353746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531304839	chr13:67353750-67353751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547992317	chr13:67353828-67353829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9599144	chr13:67353876-67353877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7321757	chr13:67353878-67353879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs190262318	chr13:67353880-67353881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575746885	chr13:67353939-67353940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370796883	chr13:67353977-67353978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9540908	chr13:67353979-67353980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9540909	chr13:67353981-67353982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71446823	chr13:67353982-67353983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61546419	chr13:67353983-67353984	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:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67346200-67368400	Weak transcription	Brain Hippocampus Middle	brain
2	chr13:67354400-67355600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:67354400-67355600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:67354400-67355600	Enhancers	HSMM	muscle
5	chr13:67354400-67355800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:67354600-67355600	Enhancers	HMEC	breast
7	chr13:67354600-67355600	Enhancers	Osteobl	bone
8	chr13:67354600-67355800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr13:67354800-67355200	Enhancers	Fetal Brain Female	brain
10	chr13:67354800-67355800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:67355200-67356600	Weak transcription	Fetal Brain Female	brain
12	chr13:67355400-67355800	Enhancers	HSMMtube	muscle
13	chr13:67355600-67374000	Weak transcription	HSMM	muscle
14	chr13:67355800-67357000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr13:67356800-67357000	Enhancers	Fetal Brain Female	brain
16	chr13:67357200-67357400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr13:67357200-67357600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:67362400-67364200	Enhancers	Brain Substantia Nigra	brain
19	chr13:67362600-67363400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:67363000-67363200	Enhancers	Brain Cingulate Gyrus	brain
21	chr13:67363200-67363600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr13:67363200-67369600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr13:67364200-67368400	Weak transcription	Brain Substantia Nigra	brain
24	chr13:67365000-67365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr13:67367600-67368200	Enhancers	Primary B cells from cord blood	blood
26	chr13:67368200-67368400	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr13:67368400-67368600	Enhancers	Primary B cells from cord blood	blood
28	chr13:67368400-67368600	Enhancers	Brain Substantia Nigra	brain
29	chr13:67368400-67368800	Enhancers	Brain Hippocampus Middle	brain
30	chr13:67368400-67369200	Enhancers	Primary B cells from peripheral blood	blood
31	chr13:67368400-67369200	Enhancers	Fetal Brain Male	brain
32	chr13:67368600-67368800	Flanking Active TSS	Brain Substantia Nigra	brain
33	chr13:67368600-67369000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:67368600-67369000	Enhancers	Brain Angular Gyrus	brain
35	chr13:67368600-67369000	Enhancers	Brain Anterior Caudate	brain
36	chr13:67368600-67369200	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr13:67368800-67369200	Enhancers	Brain Substantia Nigra	brain
38	chr13:67368800-67369800	Weak transcription	Brain Hippocampus Middle	brain
39	chr13:67369000-67370000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr13:67369000-67370000	Weak transcription	Brain Angular Gyrus	brain
41	chr13:67369000-67370000	Weak transcription	Brain Anterior Caudate	brain
42	chr13:67369200-67369600	Enhancers	Primary B cells from cord blood	blood
43	chr13:67369200-67369800	Weak transcription	Brain Substantia Nigra	brain
44	chr13:67369200-67370200	Weak transcription	Fetal Brain Male	brain
45	chr13:67369600-67370000	Enhancers	Brain Cingulate Gyrus	brain
46	chr13:67369800-67370000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr13:67369800-67370000	Enhancers	Brain Substantia Nigra	brain
48	chr13:67369800-67370400	Active TSS	Brain Hippocampus Middle	brain
49	chr13:67370000-67370200	Active TSS	Brain Anterior Caudate	brain
50	chr13:67370000-67370400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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