Variant report

Variant	nsv539630
Chromosome Location	chr8:60445016-60752655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1198)
CpG islands
(count:366)
Chromatin interactive
region (count:35)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:60528040-60528060	K562	blood:	n/a	n/a
2	ATF1	chr8:60543950-60544116	K562	blood:	n/a	n/a
3	ATF1	chr8:60468004-60468241	K562	blood:	n/a	n/a
4	ATF1	chr8:60522885-60522970	K562	blood:	n/a	n/a
5	ATF1	chr8:60517318-60517467	K562	blood:	n/a	n/a
6	ATF2	chr8:60489320-60489706	GM12878	blood:	n/a	n/a
7	ATF3	chr8:60467971-60468280	K562	blood:	n/a	n/a
8	BACH1	chr8:60723503-60723786	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:60529666-60529970	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:60662311-60662650	K562	blood:	n/a	n/a
11	BACH1	chr8:60662311-60662592	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:60556429-60556625	GM12878	blood:	n/a	n/a
13	BATF	chr8:60489407-60489752	GM12878	blood:	n/a	chr8:60489577-60489588
14	BCL3	chr8:60489407-60489652	GM12878	blood:	n/a	n/a
15	BRCA1	chr8:60670693-60670702	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:60668343-60668400	GM12878	blood:	n/a	n/a
17	CBX3	chr8:60529603-60530279	HCT-116	colon:	n/a	n/a
18	CBX3	chr8:60684132-60684420	HCT-116	colon:	n/a	n/a
19	CBX3	chr8:60595622-60595957	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:60595617-60595868	K562	blood:	n/a	n/a
21	CBX3	chr8:60529630-60530309	HCT-116	colon:	n/a	n/a
22	CCNT2	chr8:60468005-60468205	K562	blood:	n/a	chr8:60468068-60468088
23	CEBPB	chr8:60607249-60607673	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:60622670-60623036	Hela-S3	cervix:	n/a	chr8:60622847-60622860 chr8:60622849-60622858 chr8:60622848-60622859 chr8:60622849-60622858 chr8:60622849-60622858 chr8:60622847-60622860
25	CEBPB	chr8:60496387-60496610	K562	blood:	n/a	chr8:60496476-60496487
26	CEBPB	chr8:60525772-60525972	H1-hESC	embryonic stem cell:	n/a	chr8:60525785-60525796 chr8:60525785-60525798
27	CEBPB	chr8:60505957-60506245	K562	blood:	n/a	n/a
28	CEBPB	chr8:60468043-60468284	IMR90	lung:	n/a	chr8:60468135-60468146
29	CEBPB	chr8:60622672-60623035	H1-hESC	embryonic stem cell:	n/a	chr8:60622847-60622860 chr8:60622849-60622858 chr8:60622848-60622859 chr8:60622849-60622858 chr8:60622849-60622858 chr8:60622847-60622860
30	CEBPB	chr8:60699162-60699667	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:60517261-60517497	K562	blood:	n/a	n/a
32	CEBPB	chr8:60622621-60623023	ECC-1	luminal epithelium:	n/a	chr8:60622847-60622860 chr8:60622849-60622858 chr8:60622848-60622859 chr8:60622849-60622858 chr8:60622849-60622858 chr8:60622847-60622860
33	CEBPB	chr8:60496316-60496661	IMR90	lung:	n/a	chr8:60496476-60496487
34	CEBPB	chr8:60683016-60683180	HepG2	liver:	n/a	chr8:60683102-60683113
35	CEBPB	chr8:60658109-60658433	Hela-S3	cervix:	n/a	chr8:60658249-60658260
36	CEBPB	chr8:60613093-60613331	HepG2	liver:	n/a	chr8:60613194-60613205
37	CEBPB	chr8:60529480-60530323	HCT-116	colon:	n/a	n/a
38	CEBPB	chr8:60699218-60699721	HCT-116	colon:	n/a	n/a
39	CEBPB	chr8:60494709-60495016	K562	blood:	n/a	n/a
40	CEBPB	chr8:60494730-60494930	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr8:60658124-60658432	HepG2	liver:	n/a	chr8:60658249-60658260
42	CEBPB	chr8:60622668-60623016	A549	lung:	n/a	chr8:60622847-60622860 chr8:60622849-60622858 chr8:60622848-60622859 chr8:60622849-60622858 chr8:60622849-60622858 chr8:60622847-60622860
43	CEBPB	chr8:60529588-60530197	IMR90	lung:	n/a	n/a
44	CEBPB	chr8:60622672-60623034	HepG2	liver:	n/a	chr8:60622847-60622860 chr8:60622849-60622858 chr8:60622848-60622859 chr8:60622849-60622858 chr8:60622849-60622858 chr8:60622847-60622860
45	CEBPB	chr8:60589022-60589292	K562	blood:	n/a	n/a
46	CEBPB	chr8:60607207-60607690	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr8:60658127-60658425	IMR90	lung:	n/a	chr8:60658249-60658260
48	CEBPB	chr8:60494684-60495035	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:60467943-60468336	K562	blood:	n/a	chr8:60468135-60468146
50	CEBPB	chr8:60699110-60699763	HCT-116	colon:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:60589828-60589878	HEEpiC	esophagus:	n/a
2	chr8:60537981-60538031	GM19239	blood:	n/a
3	chr8:60589828-60589878	ECC-1	luminal epithelium:	n/a
4	chr8:60609179-60609229	HIPEpiC	eye:	n/a
5	chr8:60537981-60538031	HepG2	liver:	n/a
6	chr8:60609179-60609229	SK-N-SH_RA	brain:	n/a
7	chr8:60589828-60589878	Hepatocyte	liver:	n/a
8	chr8:60674791-60674841	AG09309	skin:	n/a
9	chr8:60627336-60627386	NT2-D1	testis:	n/a
10	chr8:60589828-60589878	MCF-7	breast:	n/a
11	chr8:60627336-60627386	HMEC	breast:	n/a
12	chr8:60674791-60674841	GM06990	blood:	n/a
13	chr8:60537981-60538031	SK-N-SH_RA	brain:	n/a
14	chr8:60589828-60589878	AoSMC	blood vessel:	n/a
15	chr8:60627336-60627386	GM12892	blood:	n/a
16	chr8:60609179-60609229	AoSMC	blood vessel:	n/a
17	chr8:60531025-60531075	HCM	heart:	n/a
18	chr8:60674791-60674841	HCM	heart:	n/a
19	chr8:60531025-60531075	AG09319	gingival:	n/a
20	chr8:60531025-60531075	GM19239	blood:	n/a
21	chr8:60537981-60538031	HRPEpiC	eye:	n/a
22	chr8:60531025-60531075	Hela-S3	cervix:	n/a
23	chr8:60537981-60538031	NT2-D1	testis:	n/a
24	chr8:60589828-60589878	Caco-2	colon:	n/a
25	chr8:60627336-60627386	SK-N-SH_RA	brain:	n/a
26	chr8:60537981-60538031	Hela-S3	cervix:	n/a
27	chr8:60627336-60627386	HUVEC	blood vessel:	n/a
28	chr8:60627336-60627386	CMK	blood:	n/a
29	chr8:60531025-60531075	SK-N-MC	brain:	n/a
30	chr8:60627336-60627386	H1-hESC	embryonic stem cell:	embryo
31	chr8:60537981-60538031	AG04450	lung:	fetal
32	chr8:60609179-60609229	Hela-S3	cervix:	n/a
33	chr8:60627336-60627386	K562	blood:	n/a
34	chr8:60589828-60589878	HepG2	liver:	n/a
35	chr8:60589828-60589878	HMEC	breast:	n/a
36	chr8:60674791-60674841	HCF	heart:	n/a
37	chr8:60589828-60589878	NHDF-neo	bronchial:	n/a
38	chr8:60537981-60538031	H1-hESC	embryonic stem cell:	embryo
39	chr8:60589828-60589878	SKMC	muscle:	n/a
40	chr8:60627336-60627386	Hepatocyte	liver:	n/a
41	chr8:60537981-60538031	NHDF-neo	bronchial:	n/a
42	chr8:60609179-60609229	BJ	skin:	n/a
43	chr8:60531025-60531075	Jurkat	blood:	n/a
44	chr8:60627336-60627386	HEK293	kidney:	embryo
45	chr8:60537981-60538031	NHBE	bronchial:	n/a
46	chr8:60674791-60674841	HAEpiC	amniotic membrane:	n/a
47	chr8:60627336-60627386	AG09309	skin:	n/a
48	chr8:60531025-60531075	Hepatocyte	liver:	n/a
49	chr8:60531025-60531075	Caco-2	colon:	n/a
50	chr8:60589828-60589878	HUVEC	blood vessel:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:60578488..60580541-chr8:60587371..60589170,2	K562	blood:
2	chr8:60738423..60740375-chr8:60748567..60750764,2	K562	blood:
3	chr8:60555606..60557604-chr8:60636589..60639437,2	MCF-7	breast:
4	chr8:60578488..60580541-chr8:60587371..60589170,2	K562	blood:
5	chr8:60581730..60584426-chr8:60598883..60600498,2	K562	blood:
6	chr8:60568004..60570387-chr8:60577772..60580644,2	MCF-7	breast:
7	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
8	chr8:60491495..60494237-chr8:60524811..60527779,2	K562	blood:
9	chr8:60655022..60657842-chr8:60658426..60661033,2	K562	blood:
10	chr8:60569526..60571045-chr8:60571365..60573106,2	MCF-7	breast:
11	chr8:60594445..60596869-chr8:60610407..60613088,2	K562	blood:
12	chr8:60535322..60536941-chr8:60538447..60540477,2	K562	blood:
13	chr8:60569526..60571045-chr8:60571365..60573106,2	MCF-7	breast:
14	chr8:60535322..60536941-chr8:60538447..60540477,2	K562	blood:
15	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
16	chr8:60699554..60701711-chr8:60710217..60711758,2	K562	blood:
17	chr8:60588955..60591731-chr8:60598413..60600788,2	K562	blood:
18	chr7:100026306..100026939-chr8:60670573..60671075,2	NB4	blood:
19	chr8:60581730..60584426-chr8:60598883..60600498,2	K562	blood:
20	chr8:60740494..60743423-chr8:60825234..60828198,2	K562	blood:
21	chr8:60505094..60507330-chr8:60508230..60511083,3	K562	blood:
22	chr8:60568709..60570705-chr8:60604991..60607479,2	K562	blood:
23	chr8:60738423..60740375-chr8:60748567..60750764,2	K562	blood:
24	chr8:60588955..60591731-chr8:60598413..60600788,2	K562	blood:
25	chr8:43092428..43092930-chr8:60597476..60597977,2	MCF-7	breast:
26	chr8:60555606..60557604-chr8:60636589..60639437,2	MCF-7	breast:
27	chr16:73499670..73500216-chr8:60644024..60644544,2	MCF-7	breast:
28	chr8:60568709..60570705-chr8:60604991..60607479,2	K562	blood:
29	chr8:60568004..60570387-chr8:60577772..60580644,2	MCF-7	breast:
30	chr8:60594445..60596869-chr8:60610407..60613088,2	K562	blood:
31	chr8:60536802..60538571-chr8:60542161..60544626,2	K562	blood:
32	chr8:60655022..60657842-chr8:60658426..60661033,2	K562	blood:
33	chr8:60699554..60701711-chr8:60710217..60711758,2	K562	blood:
34	chr8:60536802..60538571-chr8:60542161..60544626,2	K562	blood:
35	chr8:60491495..60494237-chr8:60524811..60527779,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOX-1	chr8:60473892-60474119	XLOC_007091
2	lnc-RAB2A-3	chr8:60519089-60519564	ENSG00000253879
3	lnc-RAB2A-3	chr8:60513937-60514011	ENSG00000253879
4	lnc-RAB2A-3	chr8:60513963-60514011	ENSG00000253879
5	lnc-RAB2A-3	chr8:60525378-60525448	ENSG00000253879
6	lnc-TOX-1	chr8:60506137-60506377	XLOC_007091
7	lnc-RAB2A-6	chr8:60733683-60733992	NONHSAT126812
8	lnc-RAB2A-7	chr8:60672606-60672822	NONHSAT126811
9	lnc-RAB2A-3	chr8:60525940-60526334	ENSG00000253879
10	lnc-TOX-4	chr8:60470087-60470414	NONHSAT126805

No data

Variant related genes	Relation type
ENSG00000253723	TF binding region
ENSG00000253879	TF binding region
ENSG00000254150	TF binding region
ENSG00000253413	TF binding region
ENSG00000253260	TF binding region
ENSG00000253723	CpG island
ENSG00000253879	CpG island
ENSG00000254150	CpG island
ENSG00000253413	CpG island
ENSG00000253260	CpG island
ENSG00000146834	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000253260	chromatin interactions

Extended variants
information (count: 5120 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5120 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16924957	chr8:60445049-60445050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141601139	chr8:60445055-60445056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528048867	chr8:60445102-60445103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181554935	chr8:60445128-60445129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142972212	chr8:60445132-60445133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531395317	chr8:60445143-60445144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375949357	chr8:60445161-60445162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184501372	chr8:60445204-60445205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532459646	chr8:60445236-60445237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10504294	chr8:60445244-60445245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559511371	chr8:60445285-60445286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201867453	chr8:60445296-60445297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368939897	chr8:60445314-60445315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530138378	chr8:60445315-60445316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144944312	chr8:60445331-60445332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570174654	chr8:60445332-60445333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148780811	chr8:60445334-60445335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552357524	chr8:60445353-60445354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565172868	chr8:60445372-60445373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570774759	chr8:60445401-60445402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535501982	chr8:60445407-60445408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535006448	chr8:60445434-60445435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553655694	chr8:60445444-60445445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79623107	chr8:60445506-60445507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189262500	chr8:60445509-60445510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115360849	chr8:60445543-60445544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143782142	chr8:60445564-60445565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72655552	chr8:60445573-60445574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577501761	chr8:60445607-60445608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543599201	chr8:60445618-60445619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565093617	chr8:60445650-60445651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577185063	chr8:60445672-60445673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2139231	chr8:60445734-60445735	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559635135	chr8:60445783-60445784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530033631	chr8:60445785-60445786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116277751	chr8:60445813-60445814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115570613	chr8:60445831-60445832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181774090	chr8:60445854-60445855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552324939	chr8:60445857-60445858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570689169	chr8:60445878-60445879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534920615	chr8:60445898-60445899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546965867	chr8:60445916-60445917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139985288	chr8:60459033-60459034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs372623361	chr8:60459034-60459035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs546348651	chr8:60459037-60459038	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs145501597	chr8:60459044-60459045	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs573510699	chr8:60459051-60459052	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs192647718	chr8:60459073-60459074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs183601488	chr8:60459077-60459078	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs529668281	chr8:60459079-60459080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Salivary gland tumor	18059337	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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60443600-60446000	Enhancers	Primary T cells from cord blood	blood
2	chr8:60443800-60445400	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr8:60443800-60445600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr8:60443800-60445800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:60443800-60445800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr8:60444200-60445200	Weak transcription	Fetal Thymus	thymus
7	chr8:60444200-60445600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:60444200-60446000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:60444400-60445400	Enhancers	Thymus	Thymus
10	chr8:60444600-60445800	Enhancers	Dnd41	blood
11	chr8:60444800-60445200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:60445000-60445400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:60445200-60445600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr8:60445200-60445800	Enhancers	Fetal Thymus	thymus
15	chr8:60445400-60445800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr8:60459000-60460000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:60459200-60460000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:60468000-60468200	Enhancers	Stomach Smooth Muscle	stomach
19	chr8:60471000-60472400	Enhancers	Fetal Heart	heart
20	chr8:60472200-60472400	Enhancers	Aorta	Aorta
21	chr8:60485000-60485200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:60489400-60489800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:60489400-60489800	Enhancers	Primary B cells from peripheral blood	blood
24	chr8:60489600-60490000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr8:60489600-60490200	Enhancers	Fetal Heart	heart
26	chr8:60491600-60492200	Enhancers	Fetal Stomach	stomach
27	chr8:60492200-60493600	Weak transcription	Fetal Stomach	stomach
28	chr8:60493400-60494000	Enhancers	Rectal Smooth Muscle	rectum
29	chr8:60493600-60494000	Enhancers	Colon Smooth Muscle	Colon
30	chr8:60493600-60494200	Enhancers	Fetal Stomach	stomach
31	chr8:60494000-60494400	Enhancers	Osteobl	bone
32	chr8:60494000-60495400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:60498600-60499400	Enhancers	Fetal Thymus	thymus
34	chr8:60506000-60506400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:60506000-60511800	Weak transcription	Fetal Heart	heart
36	chr8:60506400-60510800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:60506800-60507000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:60507000-60509800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:60507400-60507600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:60507400-60508000	Enhancers	HUVEC	blood vessel
41	chr8:60507600-60508600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr8:60508400-60509200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:60508400-60509400	Enhancers	Osteobl	bone
44	chr8:60508400-60509600	Enhancers	Brain Germinal Matrix	brain
45	chr8:60508400-60509600	Enhancers	NHDF-Ad	bronchial
46	chr8:60508600-60509400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:60509000-60509600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:60509200-60509600	Enhancers	NHLF	lung
49	chr8:60509800-60511000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:60510600-60511000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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