Variant report

Variant	esv3445521
Chromosome Location	chr8:63989447-64017270
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:917)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63997253-63997844	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:64013451-64014539	HepG2	liver:	n/a	n/a
3	ATF1	chr8:64008319-64008516	K562	blood:	n/a	n/a
4	BACH1	chr8:63998473-63998876	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr8:63998038-63998204	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr8:63997945-63998026	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:64010515-64010578	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:64015460-64015654	HepG2	liver:	n/a	chr8:64015538-64015549
9	CEBPB	chr8:63996631-63997353	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:64015353-64015647	A549	lung:	n/a	chr8:64015538-64015549
11	CEBPB	chr8:63998697-63998819	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:64001239-64001487	K562	blood:	n/a	chr8:64001374-64001385
13	CEBPB	chr8:64001276-64001476	H1-hESC	embryonic stem cell:	n/a	chr8:64001374-64001385
14	CEBPB	chr8:64001234-64001556	HepG2	liver:	n/a	chr8:64001374-64001385
15	CEBPB	chr8:64014291-64014711	HepG2	liver:	n/a	chr8:64014518-64014529
16	CHD1	chr8:63998425-63998807	H1-hESC	embryonic stem cell:	n/a	chr8:63998633-63998643
17	CHD2	chr8:63998374-63998504	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr8:64013599-64014047	HepG2	liver:	n/a	n/a
19	CTBP2	chr8:63998443-63999051	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:64002580-64002730	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr8:63998421-63998559	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:63998443-63998535	A549	lung:	n/a	n/a
23	CTCF	chr8:64015520-64015670	GM12875	blood:	n/a	n/a
24	CTCF	chr8:63990499-63990558	ProgFib	skin:	n/a	n/a
25	CTCF	chr8:63998516-63998595	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:63998534-63998538	Fibrobl	skin:	n/a	n/a
27	CTCF	chr8:63998557-63998596	Fibrobl	skin:	n/a	n/a
28	CTCF	chr8:63998240-63998390	Caco-2	colon:	n/a	n/a
29	CTCF	chr8:64002656-64002758	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr8:64002560-64002710	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:64002620-64002770	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr8:64002600-64002750	HMEC	breast:	n/a	n/a
33	CTCF	chr8:64012228-64012259	Pancreas_OC	pancreas:	n/a	n/a
34	E2F4	chr8:63998553-63998704	MCF10A-Er-Src	breast:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
35	E2F4	chr8:63989452-63989633	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr8:63997851-63998051	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:64013434-64013603	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr8:63998219-63998842	H1-hESC	embryonic stem cell:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
39	E2F6	chr8:63998426-63998850	A549	lung:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
40	E2F6	chr8:63998399-63998986	A549	lung:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
41	EBF1	chr8:63998480-63998759	GM12878	blood:	n/a	n/a
42	EP300	chr8:64005052-64005233	HepG2	liver:	n/a	n/a
43	EP300	chr8:63998124-63998188	HepG2	liver:	n/a	n/a
44	EP300	chr8:64013627-64014076	HepG2	liver:	n/a	chr8:64013749-64013759
45	EP300	chr8:64013626-64013967	HepG2	liver:	n/a	chr8:64013749-64013759
46	FOS	chr8:63998928-63999124	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:63997859-63997898	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:63998988-63999198	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL2	chr8:64005019-64005226	HepG2	liver:	n/a	chr8:64005124-64005135
50	FOSL2	chr8:64005027-64005265	HepG2	liver:	n/a	chr8:64005124-64005135

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63998640-63998690	Caco-2	colon:	n/a
2	chr8:63999030-63999080	BE2_C	brain:	n/a
3	chr8:63998640-63998690	Caco-2	colon:	n/a
4	chr8:63999030-63999080	BE2_C	brain:	n/a
5	chr8:63998778-63998828	CMK	blood:	n/a
6	chr8:63998667-63998717	BJ	skin:	n/a
7	chr8:63998463-63998513	AG04450	lung:	fetal
8	chr8:63998778-63998828	GM06990	blood:	n/a
9	chr8:63999003-63999053	NT2-D1	testis:	n/a
10	chr8:63998667-63998717	NB4	blood:	n/a
11	chr8:63998667-63998717	HCT-116	colon:	n/a
12	chr8:63997977-63998027	CMK	blood:	n/a
13	chr8:63998463-63998513	SK-N-SH	brain:	n/a
14	chr8:63999202-63999252	Hela-S3	cervix:	n/a
15	chr8:63997977-63998027	GM12891	blood:	n/a
16	chr8:63999003-63999053	HNPCEpiC	eye:	n/a
17	chr8:63998327-63998377	HCM	heart:	n/a
18	chr8:64002124-64002174	AG04449	skin:	fetal
19	chr8:63997977-63998027	HCF	heart:	n/a
20	chr8:63998778-63998828	HCM	heart:	n/a
21	chr8:63999030-63999080	HRCEpiC	kidney:	n/a
22	chr8:64002124-64002174	HCT-116	colon:	n/a
23	chr8:63998667-63998717	IMR90	lung:	fetal
24	chr8:63999003-63999053	IMR90	lung:	fetal
25	chr8:63998164-63998214	ProgFib	skin:	n/a
26	chr8:63999003-63999053	SK-N-SH_RA	brain:	n/a
27	chr8:63998649-63998699	SK-N-MC	brain:	n/a
28	chr8:63998327-63998377	SAEC	small airway:	n/a
29	chr8:63998463-63998513	T-47D	breast:	n/a
30	chr8:63999030-63999080	PFSK-1	brain:	n/a
31	chr8:64002124-64002174	A549	lung:	n/a
32	chr8:63999202-63999252	IMR90	lung:	fetal
33	chr8:63998649-63998699	HIPEpiC	eye:	n/a
34	chr8:63998778-63998828	PrEC	prostate:	n/a
35	chr8:63998667-63998717	PrEC	prostate:	n/a
36	chr8:63998667-63998717	AG04449	skin:	fetal
37	chr8:63998228-63998278	PFSK-1	brain:	n/a
38	chr8:63998778-63998828	H1-hESC	embryonic stem cell:	embryo
39	chr8:63998327-63998377	HEEpiC	esophagus:	n/a
40	chr8:63998649-63998699	HCPEpiC	choroid plexus:	n/a
41	chr8:63999202-63999252	MCF-7	breast:	n/a
42	chr8:63998649-63998699	SKMC	muscle:	n/a
43	chr8:63998228-63998278	HIPEpiC	eye:	n/a
44	chr8:63998228-63998278	BJ	skin:	n/a
45	chr8:63998667-63998717	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:63998778-63998828	T-47D	breast:	n/a
47	chr8:63998164-63998214	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:63998649-63998699	PrEC	prostate:	n/a
49	chr8:64002124-64002174	BJ	skin:	n/a
50	chr8:63997977-63998027	NH-A	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:63949699..63952423-chr8:63997523..63999992,2	K562	blood:
2	chr8:63995378..63997013-chr8:63999187..64001966,2	K562	blood:
3	chr8:64015519..64018210-chr8:64080203..64082680,2	K562	blood:
4	chr8:64017039..64019542-chr8:64021358..64023384,2	K562	blood:
5	chr8:63951421..63954662-chr8:63987305..63990409,3	K562	blood:
6	chr8:63995378..63997013-chr8:63999187..64001966,2	K562	blood:
7	chr8:63983680..63986260-chr8:63995711..63998023,2	MCF-7	breast:
8	chr8:63996810..63998343-chr8:64003518..64005481,2	K562	blood:
9	chr8:63996810..63998343-chr8:64003518..64005481,2	K562	blood:
10	chr8:63950069..63952677-chr8:64006694..64009154,2	K562	blood:

No data

Variant related genes	Relation type
TTPA	TF binding region
TTPA	CpG island
ENSG00000270673	chromatin interactions
ENSG00000137563	chromatin interactions
ENSG00000185728	chromatin interactions

Extended variants
information (count: 1078 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13255332	chr8:63989474-63989475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs13257712	chr8:63989483-63989484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs13255614	chr8:63989497-63989498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs13255357	chr8:63989499-63989500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs13255365	chr8:63989506-63989507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536340509	chr8:63989516-63989517	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532410872	chr8:63989537-63989538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs72659825	chr8:63989570-63989571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs13255661	chr8:63989582-63989583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs79266236	chr8:63989589-63989590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550311358	chr8:63989597-63989598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144676612	chr8:63989598-63989599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548684985	chr8:63989604-63989605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570280648	chr8:63989618-63989619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs13258101	chr8:63989621-63989622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs13256464	chr8:63989624-63989625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs180858443	chr8:63989635-63989636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186534221	chr8:63989659-63989660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552600968	chr8:63989688-63989689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147907010	chr8:63989762-63989763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140430406	chr8:63989763-63989764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188700844	chr8:63989788-63989789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181122918	chr8:63989801-63989802	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552597416	chr8:63989802-63989803	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377066787	chr8:63989826-63989827	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150396152	chr8:63989895-63989896	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145213359	chr8:63989910-63989911	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186165398	chr8:63989911-63989912	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs367727823	chr8:63989917-63989918	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545942914	chr8:63989947-63989948	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557658024	chr8:63989955-63989956	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111564140	chr8:63989971-63989972	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573135968	chr8:63989978-63989979	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540511153	chr8:63989982-63989983	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559818634	chr8:63989990-63989991	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190518028	chr8:63989991-63989992	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549546814	chr8:63990008-63990009	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs148900410	chr8:63990011-63990012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145608060	chr8:63990064-63990065	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs137973503	chr8:63990079-63990080	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552777725	chr8:63990084-63990085	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570956169	chr8:63990085-63990086	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78610244	chr8:63990107-63990108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183999223	chr8:63990131-63990132	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs115753700	chr8:63990148-63990149	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567737549	chr8:63990214-63990215	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116815749	chr8:63990266-63990267	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556645404	chr8:63990330-63990331	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142578068	chr8:63990340-63990341	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187291719	chr8:63990342-63990343	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63977800-63989800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:63985800-63989800	Enhancers	Liver	Liver
3	chr8:63989000-63989800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:63989800-63990000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:63989800-63990200	Flanking Active TSS	Liver	Liver
6	chr8:63989800-63990600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:63990000-63996600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:63990200-63990800	Enhancers	Liver	Liver
9	chr8:63990800-63991200	Flanking Active TSS	Liver	Liver
10	chr8:63991200-63992000	Enhancers	Liver	Liver
11	chr8:63992000-63995800	Weak transcription	Liver	Liver
12	chr8:63995800-63996000	Flanking Active TSS	Liver	Liver
13	chr8:63996000-63996400	Active TSS	Liver	Liver
14	chr8:63996400-63997200	Flanking Active TSS	Liver	Liver
15	chr8:63996600-63997600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:63996800-63997800	Enhancers	HepG2	liver
17	chr8:63997200-63998800	Active TSS	Liver	Liver
18	chr8:63997400-63997600	Enhancers	Adipose Nuclei	Adipose
19	chr8:63997400-63997600	Bivalent Enhancer	Brain Substantia Nigra	brain
20	chr8:63997400-63997600	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:63997400-63998000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:63997400-63998800	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr8:63997400-63999200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:63997400-63999200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:63997600-63997800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr8:63997600-63997800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:63997600-63997800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:63997600-63997800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:63997600-63997800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:63997600-63997800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:63997600-63997800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
32	chr8:63997600-63997800	Enhancers	Brain Cingulate Gyrus	brain
33	chr8:63997600-63997800	Enhancers	Brain Germinal Matrix	brain
34	chr8:63997600-63997800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:63997600-63997800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr8:63997600-63997800	Enhancers	Fetal Intestine Small	intestine
37	chr8:63997600-63997800	Bivalent Enhancer	Fetal Lung	lung
38	chr8:63997600-63997800	Active TSS	Stomach Smooth Muscle	stomach
39	chr8:63997600-63997800	Enhancers	NH-A	brain
40	chr8:63997600-63998000	Enhancers	Pancreas	Pancrea
41	chr8:63997600-63998000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr8:63997600-63998200	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr8:63997600-63998200	Bivalent/Poised TSS	Brain Substantia Nigra	brain
44	chr8:63997600-63998600	Active TSS	Fetal Muscle Trunk	muscle
45	chr8:63997600-63999000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:63997600-63999000	Active TSS	A549	lung
47	chr8:63997600-63999200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
48	chr8:63997600-63999200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr8:63997600-63999200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr8:63997600-63999200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain

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