Variant report

Variant	esv1803161
Chromosome Location	chr8:17135287-17155811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:183 , 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	chr8:17142585-17142622	K562	blood:	n/a	n/a
2	CEBPB	chr8:17141545-17141764	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr8:17141447-17141810	IMR90	lung:	n/a	n/a
4	CEBPB	chr8:17143949-17143999	HepG2	liver:	n/a	chr8:17143968-17143979
5	CEBPB	chr8:17142470-17142562	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr8:17142380-17142530	HBMEC	blood vessel:	n/a	n/a
7	CTCF	chr8:17135520-17135670	HPF	lung:	n/a	n/a
8	CTCF	chr8:17135560-17135710	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr8:17142416-17142593	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr8:17142440-17142590	Caco-2	colon:	n/a	n/a
11	CTCF	chr8:17135540-17135690	AG04449	skin:	n/a	n/a
12	CTCF	chr8:17135500-17135650	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr8:17135480-17135630	BJ	skin:	n/a	n/a
14	CTCF	chr8:17135540-17135690	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr8:17142420-17142570	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr8:17135500-17135650	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr8:17142420-17142570	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr8:17135524-17135627	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr8:17142520-17142670	BE2_C	brain:	n/a	n/a
20	CTCF	chr8:17142240-17142390	A549	lung:	n/a	n/a
21	CTCF	chr8:17142420-17142570	BJ	skin:	n/a	n/a
22	CTCF	chr8:17142420-17142570	BE2_C	brain:	n/a	n/a
23	CTCF	chr8:17142460-17142610	BJ	skin:	n/a	n/a
24	CTCF	chr8:17135560-17135710	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr8:17135590-17135640	Gliobla	brain:	n/a	n/a
26	CTCF	chr8:17142400-17142550	HPF	lung:	n/a	n/a
27	CTCF	chr8:17135600-17135630	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:17142414-17142534	Gliobla	brain:	n/a	n/a
29	CTCF	chr8:17135500-17135650	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr8:17142391-17142592	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr8:17142440-17142590	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr8:17135500-17135650	HMEC	breast:	n/a	n/a
33	CTCF	chr8:17142380-17142530	RPTEC	kidney:	n/a	n/a
34	CTCF	chr8:17135525-17135667	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr8:17135500-17135650	HPF	lung:	n/a	n/a
36	CTCF	chr8:17135540-17135690	HMEC	breast:	n/a	n/a
37	CTCF	chr8:17142380-17142530	GM12871	blood:	n/a	n/a
38	CTCF	chr8:17142440-17142590	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr8:17135493-17135656	K562	blood:	n/a	n/a
40	CTCF	chr8:17142420-17142570	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr8:17135493-17135694	Medullo	brain:	n/a	n/a
42	CTCF	chr8:17142420-17142570	K562	blood:	n/a	n/a
43	CTCF	chr8:17135600-17135750	RPTEC	kidney:	n/a	n/a
44	CTCF	chr8:17142440-17142590	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr8:17135520-17135670	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr8:17142440-17142590	HVMF	connective:	n/a	n/a
47	CTCF	chr8:17135500-17135650	HMF	breast:	n/a	n/a
48	CTCF	chr8:17142420-17142573	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr8:17142500-17142650	HCM	heart:	n/a	n/a
50	CTCF	chr8:17135500-17135650	NHDF-neo	bronchial:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:17146201-17146251	PFSK-1	brain:	n/a
2	chr8:17146201-17146251	GM12892	blood:	n/a
3	chr8:17146201-17146251	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:17146201-17146251	HIPEpiC	eye:	n/a
5	chr8:17146201-17146251	BJ	skin:	n/a
6	chr8:17146201-17146251	AG09309	skin:	n/a
7	chr8:17146201-17146251	SK-N-SH	brain:	n/a
8	chr8:17146201-17146251	A549	lung:	n/a
9	chr8:17146201-17146251	MCF-7	breast:	n/a
10	chr8:17146201-17146251	HRCEpiC	kidney:	n/a
11	chr8:17146201-17146251	K562	blood:	n/a
12	chr8:17146201-17146251	HRPEpiC	eye:	n/a
13	chr8:17146201-17146251	HCM	heart:	n/a
14	chr8:17146201-17146251	GM06990	blood:	n/a
15	chr8:17146201-17146251	ovcar-3	ovarian:	n/a
16	chr8:17146201-17146251	SK-N-MC	brain:	n/a
17	chr8:17146201-17146251	AG04449	skin:	fetal
18	chr8:17146201-17146251	LNCaP	prostate:	n/a
19	chr8:17146201-17146251	AG09319	gingival:	n/a
20	chr8:17146201-17146251	H1-hESC	embryonic stem cell:	embryo
21	chr8:17146201-17146251	HEK293	kidney:	embryo
22	chr8:17146201-17146251	T-47D	breast:	n/a
23	chr8:17146201-17146251	HAEpiC	amniotic membrane:	n/a
24	chr8:17146201-17146251	Jurkat	blood:	n/a
25	chr8:17146201-17146251	HEEpiC	esophagus:	n/a
26	chr8:17146201-17146251	HNPCEpiC	eye:	n/a
27	chr8:17146201-17146251	GM19239	blood:	n/a
28	chr8:17146201-17146251	NT2-D1	testis:	n/a
29	chr8:17146201-17146251	GM12891	blood:	n/a
30	chr8:17146201-17146251	SAEC	small airway:	n/a
31	chr8:17146201-17146251	NHDF-neo	bronchial:	n/a
32	chr8:17146201-17146251	AG10803	skin:	n/a
33	chr8:17146201-17146251	Hepatocyte	liver:	n/a
34	chr8:17146201-17146251	HCF	heart:	n/a
35	chr8:17146201-17146251	CMK	blood:	n/a
36	chr8:17146201-17146251	HCPEpiC	choroid plexus:	n/a
37	chr8:17146201-17146251	NH-A	brain:	n/a
38	chr8:17146201-17146251	HCT-116	colon:	n/a
39	chr8:17146201-17146251	GM12878	blood:	n/a
40	chr8:17146201-17146251	HUVEC	blood vessel:	n/a
41	chr8:17146201-17146251	Caco-2	colon:	n/a
42	chr8:17146201-17146251	AG04450	lung:	fetal
43	chr8:17146201-17146251	HL-60	blood:	n/a
44	chr8:17146201-17146251	MCF10A-Er-Src	breast:	n/a
45	chr8:17146201-17146251	RPTEC	kidney:	n/a
46	chr8:17146201-17146251	Hela-S3	cervix:	n/a
47	chr8:17146201-17146251	ProgFib	skin:	n/a
48	chr8:17146201-17146251	HMEC	breast:	n/a
49	chr8:17146201-17146251	PANC-1	pancreas:	n/a
50	chr8:17146201-17146251	NHBE	bronchial:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
2	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
3	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
4	chr8:17135210..17137746-chr8:17141581..17143958,2	MCF-7	breast:
5	chr8:17131674..17134373-chr8:17137994..17139635,2	K562	blood:
6	chr8:17058189..17058716-chr8:17135256..17136231,2	MCF-7	breast:
7	chr8:17150961..17152900-chr8:17155018..17157841,2	K562	blood:
8	chr8:17102961..17105820-chr8:17133124..17135728,2	MCF-7	breast:
9	chr8:17129178..17133989-chr8:17134678..17139635,6	K562	blood:
10	chr8:17103075..17105052-chr8:17136390..17138704,2	K562	blood:
11	chr8:17135271..17136170-chr8:17186836..17187820,2	MCF-7	breast:
12	chr8:17135640..17137186-chr8:17138924..17140760,2	K562	blood:
13	chr8:17135640..17137186-chr8:17138924..17140760,2	K562	blood:
14	chr8:17135210..17137746-chr8:17141581..17143958,2	MCF-7	breast:
15	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
16	chr8:17012171..17015039-chr8:17137782..17140431,2	K562	blood:
17	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
18	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VPS37A	hsa-miR-148b-3p	chr8:17152675-17152702

Variant related genes	Relation type
VPS37A	TF binding region
VPS37A	CpG island
ENSG00000155975	chromatin interactions
ENSG00000104219	chromatin interactions
ENSG00000198791	chromatin interactions

Extended variants
information (count: 986 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:986 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7007448	chr8:17135287-17135288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548025202	chr8:17135288-17135289	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs568037814	chr8:17135314-17135315	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536601129	chr8:17135357-17135358	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148631539	chr8:17135371-17135372	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77619061	chr8:17135372-17135373	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556999861	chr8:17135396-17135397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs34036740	chr8:17135408-17135409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs67718316	chr8:17135410-17135411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs201921917	chr8:17135412-17135413	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572672799	chr8:17135421-17135422	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571132049	chr8:17135435-17135436	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34025152	chr8:17135448-17135449	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs540152623	chr8:17135489-17135490	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546527612	chr8:17135498-17135499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573388043	chr8:17135499-17135500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144062402	chr8:17135615-17135616	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371355687	chr8:17135616-17135617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73208572	chr8:17135642-17135643	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs369062563	chr8:17135654-17135655	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs544170541	chr8:17135669-17135670	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs74877208	chr8:17135678-17135679	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576708056	chr8:17135701-17135702	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs141374796	chr8:17135844-17135845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192342047	chr8:17135848-17135849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566829878	chr8:17135876-17135877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs142452822	chr8:17135934-17135935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs9644664	chr8:17135976-17135977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs530645531	chr8:17135982-17135983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149059809	chr8:17136000-17136001	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570497595	chr8:17136010-17136011	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140422709	chr8:17136013-17136014	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541978512	chr8:17136085-17136086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181429921	chr8:17136094-17136095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567047790	chr8:17136102-17136103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74765669	chr8:17136114-17136115	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555947871	chr8:17136146-17136147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150409271	chr8:17136222-17136223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138358953	chr8:17136224-17136225	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185962703	chr8:17136239-17136240	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575397970	chr8:17136258-17136259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376071036	chr8:17136291-17136292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577661589	chr8:17136317-17136318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577396016	chr8:17136344-17136345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550280230	chr8:17136387-17136388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538337657	chr8:17136406-17136407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372921021	chr8:17136420-17136421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559343307	chr8:17136437-17136438	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573093796	chr8:17136442-17136443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560104361	chr8:17136459-17136460	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	17603634	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Colorectal cancer	17229543	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Cancer	18840272	CNVD
Epithelial cancer	20478067	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Intracranial arachnoid cysts	17641416	CNVD
Breast cancer	19287154	CNVD
Breast cancer	21956041	CNVD
Gastric adenocarcinoma	19115996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	17217626	CNVD
Cervical cancer	16585170	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Schizophrenia	19197363	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:17106000-17135400	Weak transcription	Fetal Heart	heart
2	chr8:17114400-17157200	Weak transcription	Stomach Mucosa	stomach
3	chr8:17117600-17145200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:17121800-17170600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:17122000-17152000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:17123000-17141800	Weak transcription	Small Intestine	intestine
7	chr8:17124000-17149400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:17124000-17162400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:17124400-17147600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr8:17124600-17145600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:17124800-17145400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:17125000-17164200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:17125200-17161000	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr8:17125400-17146800	Strong transcription	Dnd41	blood
15	chr8:17125600-17145200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:17125600-17145200	Weak transcription	Colonic Mucosa	Colon
17	chr8:17125600-17163600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:17125800-17145200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:17125800-17162000	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr8:17126000-17145200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:17126000-17145800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:17126000-17148600	Strong transcription	Liver	Liver
23	chr8:17126600-17148200	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr8:17126600-17148400	Strong transcription	Placenta	Placenta
25	chr8:17126600-17160200	Strong transcription	Duodenum Mucosa	Duodenum
26	chr8:17126800-17146600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr8:17128200-17142600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr8:17128400-17145200	Weak transcription	Right Ventricle	heart
29	chr8:17128600-17144600	Weak transcription	Spleen	Spleen
30	chr8:17129800-17142200	Weak transcription	Fetal Intestine Small	intestine
31	chr8:17129800-17145200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:17130600-17148200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr8:17130600-17160600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:17131200-17145800	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr8:17131200-17149800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr8:17131400-17148400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:17131400-17148800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr8:17131400-17150200	Strong transcription	Muscle Satellite Cultured Cells	--
39	chr8:17131400-17174600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr8:17131600-17136000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
41	chr8:17131600-17141000	Strong transcription	Primary hematopoietic stem cells	blood
42	chr8:17131600-17145200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:17131600-17147200	Strong transcription	Adipose Nuclei	Adipose
44	chr8:17131600-17154000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr8:17131800-17137200	Strong transcription	Primary B cells from cord blood	blood
46	chr8:17131800-17137800	Strong transcription	Primary T cells from cord blood	blood
47	chr8:17131800-17138200	Strong transcription	Fetal Muscle Trunk	muscle
48	chr8:17131800-17140200	Strong transcription	HepG2	liver
49	chr8:17131800-17140800	Strong transcription	NH-A	brain
50	chr8:17131800-17144800	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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