Variant report

Variant	nsv470031
Chromosome Location	chr4:46982218-47006399
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	chr4:46995515-46995872	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr4:47004748-47004902	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:46982870-46982896	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:46996208-46996468	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:46996198-46996533	IMR90	lung:	n/a	n/a
6	CTCF	chr4:47004760-47004910	AG04449	skin:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
7	CTCF	chr4:47004800-47004950	GM12874	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
8	CTCF	chr4:47004782-47004880	GM10248	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
9	CTCF	chr4:47004758-47004898	HUVEC	blood vessel:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
10	CTCF	chr4:47004680-47004830	BJ	skin:	n/a	n/a
11	CTCF	chr4:47004750-47004908	Pancreas_OC	pancreas:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
12	CTCF	chr4:47004660-47004810	A549	lung:	n/a	n/a
13	CTCF	chr4:47004700-47004850	AG04449	skin:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
14	CTCF	chr4:47004740-47004890	AoAF	blood vessel:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
15	CTCF	chr4:47004760-47004910	AG10803	skin:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
16	CTCF	chr4:47004720-47004870	GM12867	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
17	CTCF	chr4:47004760-47004910	WI-38	lung:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
18	CTCF	chr4:47004740-47004890	GM12873	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
19	CTCF	chr4:47004720-47004870	Caco-2	colon:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
20	CTCF	chr4:47004762-47004866	HepG2	liver:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
21	CTCF	chr4:47004740-47004890	SAEC	small airway:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
22	CTCF	chr4:47004740-47004890	HRE	kidney:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
23	CTCF	chr4:47004760-47004910	HVMF	connective:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
24	CTCF	chr4:47004720-47004870	HAc	cerebellar:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
25	CTCF	chr4:46995432-46995461	Fibrobl	skin:	n/a	n/a
26	CTCF	chr4:47004740-47004890	HepG2	liver:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
27	CTCF	chr4:47004777-47004857	MCF-7	breast:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
28	CTCF	chr4:47004681-47004968	H1-hESC	embryonic stem cell:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
29	CTCF	chr4:47004760-47004910	HBMEC	blood vessel:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
30	CTCF	chr4:47004720-47004870	Hela-S3	cervix:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
31	CTCF	chr4:47004760-47004910	HCPEpiC	choroid plexus:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
32	CTCF	chr4:47004800-47004950	HA-sp	spinal cord:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
33	CTCF	chr4:47004800-47004950	GM06990	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
34	CTCF	chr4:47004720-47004870	AG04450	lung:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
35	CTCF	chr4:47004633-47005025	IMR90	lung:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
36	CTCF	chr4:47004780-47004847	LNCaP	prostate:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
37	CTCF	chr4:47004780-47004930	NHLF	lung:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
38	CTCF	chr4:47004800-47004950	HRPEpiC	eye:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
39	CTCF	chr4:47004740-47004890	HPF	lung:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
40	CTCF	chr4:47004759-47004899	GM13977	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
41	CTCF	chr4:47005680-47005830	K562	blood:	n/a	n/a
42	CTCF	chr4:47004760-47004910	RPTEC	kidney:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
43	CTCF	chr4:47004740-47004890	NHEK	skin:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
44	CTCF	chr4:47004720-47004870	HEEpiC	esophagus:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
45	CTCF	chr4:47004720-47004870	BJ	skin:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
46	CTCF	chr4:47004740-47004890	HCPEpiC	choroid plexus:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
47	CTCF	chr4:47004651-47005005	GM12878	blood:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
48	CTCF	chr4:47004760-47004910	HMF	breast:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
49	CTCF	chr4:47004780-47004930	RPTEC	kidney:	n/a	chr4:47004813-47004834 chr4:47004818-47004836
50	CTCF	chr4:47004760-47004910	HMEC	breast:	n/a	chr4:47004813-47004834 chr4:47004818-47004836

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:46995741-46995791	HepG2	liver:	n/a
2	chr4:46992926-46992976	HRE	kidney:	n/a
3	chr4:46995741-46995791	HepG2	liver:	n/a
4	chr4:46992926-46992976	HRE	kidney:	n/a
5	chr4:46995821-46995871	ovcar-3	ovarian:	n/a
6	chr4:46995821-46995871	HNPCEpiC	eye:	n/a
7	chr4:46995821-46995871	CMK	blood:	n/a
8	chr4:46995637-46995687	NB4	blood:	n/a
9	chr4:46994748-46994798	AG09319	gingival:	n/a
10	chr4:46995474-46995524	HL-60	blood:	n/a
11	chr4:46995203-46995253	HCPEpiC	choroid plexus:	n/a
12	chr4:46992926-46992976	SK-N-MC	brain:	n/a
13	chr4:46995203-46995253	K562	blood:	n/a
14	chr4:46995203-46995253	ProgFib	skin:	n/a
15	chr4:46995741-46995791	HCF	heart:	n/a
16	chr4:46995203-46995253	Hela-S3	cervix:	n/a
17	chr4:46996264-46996314	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:46995743-46995793	AG04450	lung:	fetal
19	chr4:46992926-46992976	Hepatocyte	liver:	n/a
20	chr4:46995743-46995793	GM12878	blood:	n/a
21	chr4:46995743-46995793	Hepatocyte	liver:	n/a
22	chr4:46995474-46995524	Jurkat	blood:	n/a
23	chr4:46995637-46995687	ECC-1	luminal epithelium:	n/a
24	chr4:46995203-46995253	HMEC	breast:	n/a
25	chr4:46995203-46995253	HRCEpiC	kidney:	n/a
26	chr4:46995743-46995793	CMK	blood:	n/a
27	chr4:46995743-46995793	AG04449	skin:	fetal
28	chr4:46992926-46992976	GM19239	blood:	n/a
29	chr4:46992926-46992976	HEK293	kidney:	embryo
30	chr4:46995203-46995253	AG04449	skin:	fetal
31	chr4:46995743-46995793	U87	brain:	n/a
32	chr4:46995689-46995739	PFSK-1	brain:	n/a
33	chr4:46995659-46995709	PANC-1	pancreas:	n/a
34	chr4:46995689-46995739	SK-N-SH	brain:	n/a
35	chr4:46995821-46995871	MCF-7	breast:	n/a
36	chr4:46994748-46994798	NHDF-neo	bronchial:	n/a
37	chr4:46994748-46994798	HCPEpiC	choroid plexus:	n/a
38	chr4:46994956-46995006	HEEpiC	esophagus:	n/a
39	chr4:46995509-46995559	HEK293	kidney:	embryo
40	chr4:46995743-46995793	T-47D	breast:	n/a
41	chr4:46994748-46994798	AG04449	skin:	fetal
42	chr4:46995509-46995559	HEEpiC	esophagus:	n/a
43	chr4:46994748-46994798	AG09309	skin:	n/a
44	chr4:46995659-46995709	SK-N-SH_RA	brain:	n/a
45	chr4:46995637-46995687	U87	brain:	n/a
46	chr4:46995821-46995871	AG04450	lung:	fetal
47	chr4:46994748-46994798	HCF	heart:	n/a
48	chr4:46995659-46995709	AG10803	skin:	n/a
49	chr4:46995689-46995739	PrEC	prostate:	n/a
50	chr4:46994956-46995006	HCM	heart:	n/a

Variant related genes	Relation type
GABRA4	TF binding region
GABRB1	TF binding region
GABRA4	CpG island
GABRB1	CpG island

Extended variants
information (count: 1025 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17641660	chr4:46982218-46982219	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577971885	chr4:46982223-46982224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79188671	chr4:46982255-46982256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80297585	chr4:46982256-46982257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75176450	chr4:46982257-46982258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146480893	chr4:46982298-46982299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10517171	chr4:46982309-46982310	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182737135	chr4:46982310-46982311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561500090	chr4:46982313-46982314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187861313	chr4:46982342-46982343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192626383	chr4:46982346-46982347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546696161	chr4:46982380-46982381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72448883	chr4:46982391-46982392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397993249	chr4:46982406-46982407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571116732	chr4:46982426-46982427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10517172	chr4:46982434-46982435	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10517173	chr4:46982496-46982497	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568790364	chr4:46982497-46982498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536178967	chr4:46982503-46982504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554310983	chr4:46982505-46982506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572725539	chr4:46982509-46982510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368840586	chr4:46982524-46982525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553439669	chr4:46982555-46982556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539121436	chr4:46982562-46982563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545379260	chr4:46982608-46982609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563698733	chr4:46982658-46982659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184657884	chr4:46982701-46982702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543358792	chr4:46982723-46982724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561437434	chr4:46982746-46982747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553492826	chr4:46982759-46982760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573375590	chr4:46982765-46982766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10517174	chr4:46982826-46982827	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs546920537	chr4:46982879-46982880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187604504	chr4:46982904-46982905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141063018	chr4:46982929-46982930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550538045	chr4:46982971-46982972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10517175	chr4:46982984-46982985	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs544241329	chr4:46983009-46983010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73813760	chr4:46983062-46983063	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs73813761	chr4:46983078-46983079	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573601512	chr4:46983088-46983089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192188284	chr4:46983118-46983119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533978579	chr4:46983141-46983142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558516066	chr4:46983163-46983164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184181129	chr4:46983182-46983183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145687280	chr4:46983221-46983222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138278909	chr4:46983239-46983240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372590031	chr4:46983343-46983344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75253498	chr4:46983360-46983361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543296008	chr4:46983396-46983397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46978000-46983000	Weak transcription	Fetal Brain Female	brain
2	chr4:46978400-46986400	Weak transcription	Fetal Brain Male	brain
3	chr4:46978600-46983800	Weak transcription	Brain Anterior Caudate	brain
4	chr4:46981800-46982600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr4:46982200-46983200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:46982200-46983200	Enhancers	NHEK	skin
7	chr4:46982800-46983000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr4:46982800-46983200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:46983000-46983800	Enhancers	Fetal Brain Female	brain
10	chr4:46983000-46984200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:46983600-46984000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:46983600-46984000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:46983600-46984000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:46983600-46984000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:46983600-46984200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:46983800-46984200	Enhancers	Brain Anterior Caudate	brain
17	chr4:46984200-46989000	Weak transcription	Brain Anterior Caudate	brain
18	chr4:46986400-46987000	Enhancers	Fetal Brain Male	brain
19	chr4:46987000-46990800	Weak transcription	Fetal Brain Male	brain
20	chr4:46988600-46990000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr4:46989000-46989400	Enhancers	Brain Anterior Caudate	brain
22	chr4:46989000-46989800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr4:46989200-46990000	Active TSS	Brain Angular Gyrus	brain
24	chr4:46989400-46989600	Bivalent Enhancer	Fetal Heart	heart
25	chr4:46989400-46990800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:46989400-46991200	Weak transcription	Brain Anterior Caudate	brain
27	chr4:46989600-46990400	Enhancers	Fetal Heart	heart
28	chr4:46989800-46990000	Enhancers	Fetal Intestine Small	intestine
29	chr4:46990000-46991000	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr4:46990000-46993400	Weak transcription	Brain Angular Gyrus	brain
31	chr4:46990800-46991000	Enhancers	Fetal Brain Male	brain
32	chr4:46990800-46994000	Enhancers	Fetal Heart	heart
33	chr4:46991000-46991400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr4:46991000-46992600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:46991200-46993600	Active TSS	Brain Anterior Caudate	brain
36	chr4:46991400-46991600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr4:46991400-46991600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
38	chr4:46991400-46991800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
39	chr4:46992600-46993400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:46993200-46995400	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr4:46993400-46994200	Active TSS	Brain Cingulate Gyrus	brain
42	chr4:46993400-46997400	Active TSS	Brain Angular Gyrus	brain
43	chr4:46993400-46997600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr4:46993600-46993800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:46993600-46993800	Active TSS	Brain Hippocampus Middle	brain
46	chr4:46993600-46994000	Flanking Active TSS	Brain Anterior Caudate	brain
47	chr4:46994000-46994600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr4:46994000-46994600	Bivalent Enhancer	Fetal Heart	heart
49	chr4:46994000-46997400	Active TSS	Brain Anterior Caudate	brain
50	chr4:46994200-46994400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood

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