Variant report

Variant	nsv538388
Chromosome Location	chr6:100810738-101001115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1589)
CpG islands
(count:5922)
Chromatin interactive
region (count:81)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:100951005-100951197	HepG2	liver:	n/a	n/a
2	ATF1	chr6:100814451-100814592	K562	blood:	n/a	n/a
3	ATF1	chr6:100860835-100861119	K562	blood:	n/a	n/a
4	ATF1	chr6:100832716-100832811	K562	blood:	n/a	n/a
5	ATF2	chr6:100920637-100921098	GM12878	blood:	n/a	n/a
6	ATF2	chr6:100920600-100920975	GM12878	blood:	n/a	n/a
7	ATF2	chr6:100927297-100927752	GM12878	blood:	n/a	n/a
8	BACH1	chr6:100903060-100903315	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:100998586-100998662	K562	blood:	n/a	n/a
10	BACH1	chr6:100905663-100906313	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:100909343-100909496	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:100952671-100953056	GM12878	blood:	n/a	chr6:100952874-100952885
13	BATF	chr6:100952670-100952988	GM12878	blood:	n/a	chr6:100952874-100952885
14	BATF	chr6:100923460-100923757	GM12878	blood:	n/a	n/a
15	BATF	chr6:100909923-100910152	GM12878	blood:	n/a	n/a
16	BATF	chr6:100920606-100920997	GM12878	blood:	n/a	n/a
17	BATF	chr6:100923457-100923797	GM12878	blood:	n/a	n/a
18	BCL3	chr6:100920634-100920909	GM12878	blood:	n/a	chr6:100920763-100920772
19	BCL3	chr6:100920607-100921005	GM12878	blood:	n/a	chr6:100920763-100920772
20	BCLAF1	chr6:100932205-100932651	GM12878	blood:	n/a	n/a
21	BCLAF1	chr6:100927281-100927759	GM12878	blood:	n/a	chr6:100927433-100927442
22	BHLHE40	chr6:100920642-100921047	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:100927364-100927699	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:100952276-100952378	GM12878	blood:	n/a	n/a
25	BRCA1	chr6:100831839-100831854	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr6:100903542-100903770	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr6:100911583-100911905	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:100878855-100879089	HepG2	liver:	n/a	chr6:100879030-100879043 chr6:100879031-100879042 chr6:100879030-100879043
29	CEBPB	chr6:100965649-100965740	A549	lung:	n/a	n/a
30	CEBPB	chr6:101000174-101000478	HepG2	liver:	n/a	chr6:101000302-101000313 chr6:101000302-101000315
31	CEBPB	chr6:100922982-100923119	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:100814368-100814669	A549	lung:	n/a	n/a
33	CEBPB	chr6:100875372-100875715	ECC-1	luminal epithelium:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
34	CEBPB	chr6:100929830-100930153	HepG2	liver:	n/a	chr6:100929989-100930000
35	CEBPB	chr6:100941888-100942166	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:100854488-100854763	IMR90	lung:	n/a	chr6:100854637-100854648
37	CEBPB	chr6:100875334-100875699	K562	blood:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
38	CEBPB	chr6:100814352-100814710	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:100829022-100829304	IMR90	lung:	n/a	n/a
40	CEBPB	chr6:100929814-100930155	IMR90	lung:	n/a	chr6:100929989-100930000
41	CEBPB	chr6:100875344-100875686	IMR90	lung:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
42	CEBPB	chr6:101000152-101000441	K562	blood:	n/a	chr6:101000302-101000313 chr6:101000302-101000315
43	CEBPB	chr6:100875332-100875661	MCF-7	breast:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
44	CEBPB	chr6:100922832-100923234	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:100827252-100827594	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:100922893-100923183	A549	lung:	n/a	n/a
47	CEBPB	chr6:100829058-100829326	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr6:100894518-100894546	K562	blood:	n/a	n/a
49	CEBPB	chr6:100922891-100923205	K562	blood:	n/a	n/a
50	CEBPB	chr6:100919235-100919358	A549	lung:	n/a	n/a

(count:5922 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:100906182-100906232	NH-A	brain:	n/a
2	chr6:100915395-100915445	Caco-2	colon:	n/a
3	chr6:100909121-100909171	T-47D	breast:	n/a
4	chr6:100836916-100836966	HCM	heart:	n/a
5	chr6:100911964-100912014	RPTEC	kidney:	n/a
6	chr6:100906182-100906232	NH-A	brain:	n/a
7	chr6:100915395-100915445	Caco-2	colon:	n/a
8	chr6:100909121-100909171	T-47D	breast:	n/a
9	chr6:100836916-100836966	HCM	heart:	n/a
10	chr6:100911964-100912014	RPTEC	kidney:	n/a
11	chr6:100901371-100901421	Caco-2	colon:	n/a
12	chr6:100894629-100894679	NT2-D1	testis:	n/a
13	chr6:100917871-100917921	ProgFib	skin:	n/a
14	chr6:100915634-100915684	HNPCEpiC	eye:	n/a
15	chr6:100836916-100836966	CMK	blood:	n/a
16	chr6:100894513-100894563	IMR90	lung:	fetal
17	chr6:100893665-100893715	RPTEC	kidney:	n/a
18	chr6:100904689-100904739	AG04450	lung:	fetal
19	chr6:100902470-100902520	RPTEC	kidney:	n/a
20	chr6:100915634-100915684	NHBE	bronchial:	n/a
21	chr6:100911964-100912014	HRPEpiC	eye:	n/a
22	chr6:100891601-100891651	U87	brain:	n/a
23	chr6:100920825-100920875	PrEC	prostate:	n/a
24	chr6:100904055-100904105	NT2-D1	testis:	n/a
25	chr6:100917022-100917072	HEK293	kidney:	embryo
26	chr6:100915767-100915817	U87	brain:	n/a
27	chr6:100912940-100912990	ECC-1	luminal epithelium:	n/a
28	chr6:100909121-100909171	HCPEpiC	choroid plexus:	n/a
29	chr6:100915191-100915241	SKMC	muscle:	n/a
30	chr6:100912946-100912996	HEK293	kidney:	embryo
31	chr6:100911550-100911600	U87	brain:	n/a
32	chr6:100903575-100903625	GM06990	blood:	n/a
33	chr6:100913030-100913080	GM06990	blood:	n/a
34	chr6:100894629-100894679	GM12878	blood:	n/a
35	chr6:100911744-100911794	MCF10A-Er-Src	breast:	n/a
36	chr6:100904316-100904366	ProgFib	skin:	n/a
37	chr6:100913923-100913973	AG09309	skin:	n/a
38	chr6:100914639-100914689	A549	lung:	n/a
39	chr6:100912940-100912990	HRPEpiC	eye:	n/a
40	chr6:100904689-100904739	HCT-116	colon:	n/a
41	chr6:100897445-100897495	RPTEC	kidney:	n/a
42	chr6:100911240-100911290	AG09319	gingival:	n/a
43	chr6:100895050-100895100	HEK293	kidney:	embryo
44	chr6:100895907-100895957	AG09309	skin:	n/a
45	chr6:100913923-100913973	ProgFib	skin:	n/a
46	chr6:100895143-100895193	HNPCEpiC	eye:	n/a
47	chr6:100903817-100903867	Caco-2	colon:	n/a
48	chr6:100911964-100912014	LNCaP	prostate:	n/a
49	chr6:100905038-100905088	NT2-D1	testis:	n/a
50	chr6:100904376-100904426	HMEC	breast:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:100858630..100860208-chr6:100863468..100866300,2	K562	blood:
2	chr6:100963737..100966583-chr6:100995209..100997563,2	MCF-7	breast:
3	chr6:100933157..100934125-chr6:101104912..101105845,2	MCF-7	breast:
4	chr6:100914205..100915074-chr6:100925463..100926076,2	MCF-7	breast:
5	chr6:100867794..100869514-chr6:100873709..100875237,2	K562	blood:
6	chr6:100895834..100897830-chr6:100900574..100903178,3	K562	blood:
7	chr6:100940983..100941708-chr6:100956888..100957470,2	MCF-7	breast:
8	chr6:100883478..100885403-chr6:100886324..100888180,2	K562	blood:
9	chr6:100774927..100775901-chr6:100927025..100927714,2	MCF-7	breast:
10	chr6:100449696..100450412-chr6:100926998..100927540,2	K562	blood:
11	chr6:100885282..100888001-chr6:100892746..100894898,2	K562	blood:
12	chr6:100858630..100860208-chr6:100863468..100866300,2	K562	blood:
13	chr6:100967956..100970627-chr6:100970940..100972934,2	MCF-7	breast:
14	chr6:100929215..100933103-chr6:100933926..100937760,3	K562	blood:
15	chr6:100935491..100937545-chr6:100952040..100953953,2	K562	blood:
16	chr6:100954917..100956828-chr6:100959849..100962215,2	K562	blood:
17	chr6:100831826..100835333-chr6:100836455..100839258,3	K562	blood:
18	chr6:100887121..100888891-chr6:100901432..100903601,2	MCF-7	breast:
19	chr6:100895834..100897830-chr6:100900625..100903178,2	K562	blood:
20	chr6:100940983..100941708-chr6:100956888..100957470,2	MCF-7	breast:
21	chr6:100705901..100707480-chr6:100836775..100838969,2	K562	blood:
22	chr6:100831826..100835333-chr6:100836455..100839258,3	K562	blood:
23	chr6:100908327..100910621-chr6:100914553..100916127,2	MCF-7	breast:
24	chr6:100876201..100879163-chr6:100881481..100884143,2	K562	blood:
25	chr6:100564273..100565073-chr6:100927281..100928020,3	MCF-7	breast:
26	chr6:100820119..100822622-chr6:100822669..100824422,2	MCF-7	breast:
27	chr6:100887121..100888891-chr6:100901432..100903601,2	MCF-7	breast:
28	chr6:100895834..100897830-chr6:100900625..100903178,2	K562	blood:
29	chr6:100563761..100565505-chr6:100927056..100927981,5	K562	blood:
30	chr6:100908327..100910621-chr6:100914553..100916127,2	MCF-7	breast:
31	chr6:100822946..100825730-chr6:100831670..100834406,2	MCF-7	breast:
32	chr6:100930706..100932769-chr6:100940646..100942304,2	MCF-7	breast:
33	chr6:100960099..100962319-chr6:100964454..100967453,2	K562	blood:
34	chr6:100774639..100776281-chr6:100926982..100927977,6	MCF-7	breast:
35	chr6:100869406..100871718-chr6:100874108..100875813,2	MCF-7	breast:
36	chr6:100960099..100962319-chr6:100964454..100967453,2	K562	blood:
37	chr6:100929215..100933103-chr6:100933926..100937760,3	K562	blood:
38	chr6:100924572..100926704-chr6:100927838..100930787,2	MCF-7	breast:
39	chr6:100939724..100941535-chr6:101006405..101008824,2	MCF-7	breast:
40	chr6:100854348..100856456-chr6:100877921..100879422,2	MCF-7	breast:
41	chr6:100924229..100925059-chr9:30183723..30184530,2	MCF-7	breast:
42	chr6:100906855..100909524-chr6:100935004..100937170,2	MCF-7	breast:
43	chr6:100950233..100952061-chr6:100952645..100955595,2	K562	blood:
44	chr6:100894013..100895525-chr6:100899314..100902220,2	MCF-7	breast:
45	chr6:100924572..100926704-chr6:100927838..100930787,2	MCF-7	breast:
46	chr6:100887185..100889268-chr6:100914294..100916955,2	MCF-7	breast:
47	chr6:100916462..100918120-chr6:100922266..100924903,2	MCF-7	breast:
48	chr6:100922132..100924649-chr6:100925784..100927667,2	K562	blood:
49	chr6:100927185..100927844-chr6:101105325..101105870,2	MCF-7	breast:
50	chr6:100883478..100885403-chr6:100886324..100888180,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM13-10	chr6:100951626-100955498	NONHSAT114157
2	lnc-PRDM13-4	chr6:100885132-100885360	ENSG00000228082.1
3	lnc-SIM1-1	chr6:100832891-100833225	NONHSAT114152
4	lnc-PRDM13-4	chr6:100874994-100875144	ENSG00000228082.1
5	lnc-GRIK2-7	chr6:100978152-100978928	NONHSAT114159

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ASCC3	hsa-miR-98-5p	chr6:100957150-100957170
2	ASCC3	hsa-miR-16-5p	chr6:100956913-100956934
3	ASCC3	hsa-let-7a-5p	chr6:100957150-100957170
4	ASCC3	hsa-miR-124-3p	chr6:100957172-100957191
5	ASCC3	hsa-let-7b-5p	chr6:100957150-100957171
6	ASCC3	hsa-miR-30a-5p	chr6:100956935-100956928
7	ASCC3	hsa-miR-124-3p	chr6:100957064-100957083
8	ASCC3	hsa-miR-30a-5p	chr6:100956729-100956750
9	ASCC3	hsa-miR-124-3p	chr6:100957081-100957102
10	ASCC3	hsa-miR-30a-5p	chr6:100956929-100956950

Variant related genes	Relation type
SIM1	TF binding region
ENSG00000228082	TF binding region
ASCC3	TF binding region
ENSG00000220695	TF binding region
SIM1	CpG island
ENSG00000228082	CpG island
ASCC3	CpG island
ENSG00000220695	CpG island
ENSG00000112246	chromatin interactions
ENSG00000228082	chromatin interactions
ENSG00000216378	chromatin interactions

Extended variants
information (count: 6520 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6520 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568939553	chr6:100810759-100810760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550294379	chr6:100810766-100810767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141577201	chr6:100810822-100810823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570063080	chr6:100810828-100810829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554696766	chr6:100810836-100810837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143445969	chr6:100810844-100810845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540213611	chr6:100810871-100810872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147999313	chr6:100810944-100810945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369024179	chr6:100810947-100810948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9403695	chr6:100810976-100810977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544799239	chr6:100810985-100810986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141694878	chr6:100810986-100810987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530227454	chr6:100811015-100811016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541959267	chr6:100811017-100811018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560196758	chr6:100811028-100811029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72933850	chr6:100811031-100811032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140120576	chr6:100811060-100811061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571531284	chr6:100811072-100811073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190492879	chr6:100811098-100811099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550852188	chr6:100811128-100811129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73760880	chr6:100811144-100811145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536437363	chr6:100811165-100811166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147338474	chr6:100811197-100811198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182973809	chr6:100811208-100811209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201701782	chr6:100811223-100811224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73760881	chr6:100811247-100811248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558226690	chr6:100811273-100811274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577468469	chr6:100811280-100811281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192694622	chr6:100811301-100811302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17060420	chr6:100811392-100811393	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546278034	chr6:100811412-100811413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574725121	chr6:100811413-100811414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541996078	chr6:100811450-100811451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571283668	chr6:100811459-100811460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370147630	chr6:100811470-100811471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572171126	chr6:100811471-100811472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546185768	chr6:100811508-100811509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377582148	chr6:100811522-100811523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17792983	chr6:100811533-100811534	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149760996	chr6:100811545-100811546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550637186	chr6:100811557-100811558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377112550	chr6:100811584-100811585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78602654	chr6:100811624-100811625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185043862	chr6:100811637-100811638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536634666	chr6:100811650-100811651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368607476	chr6:100811667-100811668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114027750	chr6:100811671-100811672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187459125	chr6:100811677-100811678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533605063	chr6:100811680-100811681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552245857	chr6:100811682-100811683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2290 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100809400-100811200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr6:100809400-100811600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr6:100809600-100811000	Enhancers	H1 Cell Line	embryonic stem cell
4	chr6:100809600-100811000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:100809600-100811400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:100810000-100810800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:100810000-100811000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:100810200-100811200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:100810600-100811200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:100810600-100811600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:100810800-100811000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:100810800-100811200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:100810800-100811200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:100810800-100811800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:100811000-100813600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:100811400-100812200	Enhancers	NHEK	skin
17	chr6:100811400-100812400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:100811400-100812400	Enhancers	HMEC	breast
19	chr6:100811600-100812600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr6:100811800-100820200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr6:100812200-100814200	Weak transcription	NHEK	skin
22	chr6:100812400-100814000	Weak transcription	HMEC	breast
23	chr6:100813600-100814000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:100813800-100814200	Enhancers	Aorta	Aorta
25	chr6:100813800-100815000	Enhancers	Placenta	Placenta
26	chr6:100814000-100814800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr6:100814000-100814800	Enhancers	HMEC	breast
28	chr6:100814000-100814800	Enhancers	NHDF-Ad	bronchial
29	chr6:100814000-100815000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:100814000-100815200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:100814000-100820000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:100814200-100814600	Enhancers	NHEK	skin
33	chr6:100814200-100814800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:100814200-100830000	Weak transcription	Aorta	Aorta
35	chr6:100814400-100815400	Enhancers	Hela-S3	cervix
36	chr6:100815200-100819400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:100815600-100816200	Enhancers	Dnd41	blood
38	chr6:100816200-100820000	Weak transcription	Dnd41	blood
39	chr6:100818400-100818600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:100818600-100820200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:100819400-100820200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:100819800-100820800	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr6:100820000-100820600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr6:100820000-100821000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:100820000-100821000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr6:100820000-100821000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr6:100820000-100821000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:100820000-100821000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:100820000-100821200	Enhancers	Dnd41	blood
50	chr6:100820200-100820600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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