Variant report

Variant	nsv883452
Chromosome Location	chr6:13704341-13733565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1349)
CpG islands
(count:915)
Chromatin interactive
region (count:88)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13712424-13713017	K562	blood:	n/a	chr6:13712676-13712692
2	ARID3A	chr6:13710549-13710787	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:13711049-13711203	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:13709911-13710277	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:13715820-13716305	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:13712158-13713048	HepG2	liver:	n/a	chr6:13712676-13712692
7	ARID3A	chr6:13709592-13710928	K562	blood:	n/a	n/a
8	ARID3A	chr6:13711869-13711948	HepG2	liver:	n/a	n/a
9	ATF1	chr6:13709946-13710245	K562	blood:	n/a	n/a
10	ATF2	chr6:13712194-13712654	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:13712162-13713177	GM12878	blood:	n/a	n/a
12	ATF2	chr6:13715428-13716029	GM12878	blood:	n/a	n/a
13	ATF2	chr6:13712283-13712816	GM12878	blood:	n/a	n/a
14	ATF2	chr6:13715445-13716093	GM12878	blood:	n/a	n/a
15	ATF2	chr6:13712234-13712753	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr6:13733486-13733739	K562	blood:	n/a	n/a
17	BACH1	chr6:13712053-13712635	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:13712200-13712336	K562	blood:	n/a	n/a
19	BACH1	chr6:13710641-13711213	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:13712807-13713104	GM12878	blood:	n/a	n/a
21	BATF	chr6:13712822-13713150	GM12878	blood:	n/a	n/a
22	BATF	chr6:13715475-13716015	GM12878	blood:	n/a	n/a
23	BATF	chr6:13715519-13715903	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:13715520-13715967	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:13715591-13715843	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:13711562-13712688	GM12878	blood:	n/a	chr6:13712033-13712046 chr6:13712038-13712047 chr6:13711812-13711825 chr6:13711810-13711823 chr6:13712035-13712048 chr6:13711801-13711809 chr6:13712433-13712446 chr6:13712036-13712049 chr6:13712039-13712052
27	BCLAF1	chr6:13712053-13712685	K562	blood:	n/a	chr6:13712433-13712446
28	BCLAF1	chr6:13712091-13712679	GM12878	blood:	n/a	chr6:13712433-13712446
29	BCLAF1	chr6:13711670-13712004	GM12878	blood:	n/a	chr6:13711812-13711825 chr6:13711810-13711823 chr6:13711801-13711809
30	BHLHE40	chr6:13711667-13712679	GM12878	blood:	n/a	chr6:13712430-13712446 chr6:13712033-13712049 chr6:13712296-13712312 chr6:13712027-13712043 chr6:13712039-13712055 chr6:13712036-13712052
31	BHLHE40	chr6:13733483-13733745	A549	lung:	n/a	n/a
32	BHLHE40	chr6:13710691-13711324	K562	blood:	n/a	chr6:13711105-13711121 chr6:13711102-13711118
33	BHLHE40	chr6:13733381-13733912	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:13733450-13733676	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:13712951-13713151	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:13733364-13733925	K562	blood:	n/a	n/a
37	BHLHE40	chr6:13711771-13712718	K562	blood:	n/a	chr6:13712430-13712446 chr6:13712033-13712049 chr6:13712296-13712312 chr6:13712027-13712043 chr6:13712039-13712055 chr6:13712036-13712052
38	BHLHE40	chr6:13712145-13712649	HepG2	liver:	n/a	chr6:13712430-13712446 chr6:13712296-13712312
39	BRCA1	chr6:13712056-13712543	GM12878	blood:	n/a	n/a
40	BRCA1	chr6:13711828-13712668	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:13711762-13712860	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr6:13711975-13712750	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr6:13725532-13726302	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:13725582-13726303	HCT-116	colon:	n/a	n/a
45	CBX3	chr6:13715701-13716148	K562	blood:	n/a	n/a
46	CBX3	chr6:13716704-13717035	K562	blood:	n/a	n/a
47	CBX3	chr6:13712182-13713153	K562	blood:	n/a	n/a
48	CBX3	chr6:13718289-13718748	K562	blood:	n/a	n/a
49	CCNT2	chr6:13710762-13713047	K562	blood:	n/a	chr6:13711078-13711087
50	CCNT2	chr6:13709817-13710043	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13710042-13710092	RPTEC	kidney:	n/a
2	chr6:13712555-13712605	NT2-D1	testis:	n/a
3	chr6:13711094-13711144	LNCaP	prostate:	n/a
4	chr6:13717292-13717342	HCM	heart:	n/a
5	chr6:13707062-13707112	ProgFib	skin:	n/a
6	chr6:13712555-13712605	NH-A	brain:	n/a
7	chr6:13712693-13712743	PANC-1	pancreas:	n/a
8	chr6:13715593-13715643	LNCaP	prostate:	n/a
9	chr6:13712555-13712605	ProgFib	skin:	n/a
10	chr6:13710042-13710092	Hepatocyte	liver:	n/a
11	chr6:13712174-13712224	LNCaP	prostate:	n/a
12	chr6:13711924-13711974	PrEC	prostate:	n/a
13	chr6:13717068-13717118	NHDF-neo	bronchial:	n/a
14	chr6:13711094-13711144	AG04450	lung:	fetal
15	chr6:13707062-13707112	HIPEpiC	eye:	n/a
16	chr6:13717068-13717118	HUVEC	blood vessel:	n/a
17	chr6:13717068-13717118	ECC-1	luminal epithelium:	n/a
18	chr6:13711723-13711773	AG04449	skin:	fetal
19	chr6:13712555-13712605	HRE	kidney:	n/a
20	chr6:13711938-13711988	SK-N-MC	brain:	n/a
21	chr6:13717292-13717342	Hela-S3	cervix:	n/a
22	chr6:13711924-13711974	HRE	kidney:	n/a
23	chr6:13717292-13717342	AG04450	lung:	fetal
24	chr6:13715593-13715643	AG04449	skin:	fetal
25	chr6:13712555-13712605	NB4	blood:	n/a
26	chr6:13717068-13717118	SK-N-SH	brain:	n/a
27	chr6:13707062-13707112	PrEC	prostate:	n/a
28	chr6:13715593-13715643	SAEC	small airway:	n/a
29	chr6:13711094-13711144	PFSK-1	brain:	n/a
30	chr6:13711938-13711988	Hepatocyte	liver:	n/a
31	chr6:13712174-13712224	CMK	blood:	n/a
32	chr6:13710042-13710092	NB4	blood:	n/a
33	chr6:13717292-13717342	MCF10A-Er-Src	breast:	n/a
34	chr6:13710980-13711030	CMK	blood:	n/a
35	chr6:13712693-13712743	ovcar-3	ovarian:	n/a
36	chr6:13717292-13717342	HRCEpiC	kidney:	n/a
37	chr6:13712555-13712605	HCF	heart:	n/a
38	chr6:13712555-13712605	AG10803	skin:	n/a
39	chr6:13710980-13711030	LNCaP	prostate:	n/a
40	chr6:13711723-13711773	NHDF-neo	bronchial:	n/a
41	chr6:13711723-13711773	Hela-S3	cervix:	n/a
42	chr6:13731564-13731614	ovcar-3	ovarian:	n/a
43	chr6:13707062-13707112	Hela-S3	cervix:	n/a
44	chr6:13710980-13711030	GM19239	blood:	n/a
45	chr6:13711094-13711144	GM12891	blood:	n/a
46	chr6:13711924-13711974	BJ	skin:	n/a
47	chr6:13711938-13711988	HEEpiC	esophagus:	n/a
48	chr6:13717068-13717118	HRE	kidney:	n/a
49	chr6:13712555-13712605	HCM	heart:	n/a
50	chr6:13715593-13715643	HUVEC	blood vessel:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:13726567..13730349-chr6:13731147..13734427,5	K562	blood:
2	chr6:13656880..13659020-chr6:13704232..13705741,2	K562	blood:
3	chr6:13711999..13712561-chr6:13733317..13733992,2	MCF-7	breast:
4	chr6:13727618..13729518-chr6:13729708..13731514,2	MCF-7	breast:
5	chr6:13726567..13730349-chr6:13731147..13734427,5	K562	blood:
6	chr6:13721713..13725590-chr6:13730515..13734730,4	K562	blood:
7	chr6:13724511..13727426-chr6:13727934..13730213,2	MCF-7	breast:
8	chr6:13622436..13626191-chr6:13709343..13710896,3	MCF-7	breast:
9	chr6:13710342..13712818-chr6:13812780..13815719,5	MCF-7	breast:
10	chr6:13654696..13656531-chr6:13723124..13724832,2	K562	blood:
11	chr6:13712160..13713873-chr6:13816640..13818344,2	K562	blood:
12	chr6:13710378..13713685-chr6:13811318..13818372,10	MCF-7	breast:
13	chr6:13612229..13617961-chr6:13707977..13713490,13	K562	blood:
14	chr6:13709976..13711553-chr6:13927629..13929314,2	K562	blood:
15	chr6:13703438..13706019-chr6:13706100..13707717,2	MCF-7	breast:
16	chr6:13573088..13576408-chr6:13709684..13713261,5	MCF-7	breast:
17	chr6:13711887..13713957-chr6:13747635..13751147,3	K562	blood:
18	chr6:13709798..13714586-chr6:13721714..13727470,15	MCF-7	breast:
19	chr6:13664552..13667065-chr6:13707492..13709174,2	MCF-7	breast:
20	chr6:13712294..13715235-chr6:13734842..13736345,2	K562	blood:
21	chr6:13703438..13706019-chr6:13706100..13707717,2	MCF-7	breast:
22	chr6:13617821..13621321-chr6:13710420..13713075,4	MCF-7	breast:
23	chr17:57919238..57922162-chr6:13717234..13718748,2	MCF-7	breast:
24	chr6:13713710..13717343-chr6:13751875..13754798,3	MCF-7	breast:
25	chr6:13701020..13704816-chr6:13710240..13712959,3	MCF-7	breast:
26	chr6:13709898..13716469-chr6:13809605..13815390,11	K562	blood:
27	chr20:52207726..52210399-chr6:13710282..13712059,2	MCF-7	breast:
28	chr6:13712256..13714398-chr6:13725384..13727195,2	MCF-7	breast:
29	chr6:13708783..13709718-chr6:13814193..13814871,2	K562	blood:
30	chr6:13721713..13725590-chr6:13730515..13734730,4	K562	blood:
31	chr6:13683514..13685773-chr6:13730850..13733772,2	K562	blood:
32	chr6:13707885..13710532-chr6:13710566..13713183,2	MCF-7	breast:
33	chr6:13613792..13617654-chr6:13711804..13714048,3	K562	blood:
34	chr6:13613655..13618769-chr6:13709987..13714197,10	MCF-7	breast:
35	chr12:120729387..120731467-chr6:13710748..13713061,2	MCF-7	breast:
36	chr6:13677684..13681560-chr6:13703690..13707660,4	K562	blood:
37	chr6:13613412..13615383-chr6:13705399..13707635,2	K562	blood:
38	chr6:13708644..13711231-chr6:13725404..13728369,2	MCF-7	breast:
39	chr6:13678691..13681560-chr6:13700664..13706580,5	K562	blood:
40	chr6:13667308..13669773-chr6:13712805..13714594,2	K562	blood:
41	chr6:13710738..13712943-chr6:13714753..13716732,2	MCF-7	breast:
42	chr6:13571943..13574615-chr6:13703735..13706256,3	K562	blood:
43	chr6:13733063..13736009-chr6:13738109..13740804,2	MCF-7	breast:
44	chr6:13703743..13705757-chr6:13712344..13714353,2	MCF-7	breast:
45	chr6:13711035..13715005-chr6:13727821..13730116,3	MCF-7	breast:
46	chr6:13685654..13687254-chr6:13711731..13713330,2	MCF-7	breast:
47	chr6:13693992..13697221-chr6:13708052..13711450,4	MCF-7	breast:
48	chr6:13712335..13712843-chr6:13813904..13814896,2	NB4	blood:
49	chr6:13724511..13727426-chr6:13727934..13730213,2	MCF-7	breast:
50	chr6:13615378..13616963-chr6:13714230..13716669,2	K562	blood:

No data

Variant related genes	Relation type
RANBP9	TF binding region
RANBP9	CpG island
ENSG00000112137	chromatin interactions
ENSG00000215022	chromatin interactions
ENSG00000252966	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000233075	chromatin interactions
ENSG00000268059	chromatin interactions
ENSG00000124523	chromatin interactions
ENSG00000231485	chromatin interactions
ENSG00000050393	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000010017	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000200795	chromatin interactions

Extended variants
information (count: 1373 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1373 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs204221	chr6:13704341-13704342	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148112306	chr6:13704360-13704361	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531507408	chr6:13704389-13704390	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs566104773	chr6:13704401-13704402	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548322769	chr6:13704429-13704430	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190185702	chr6:13704447-13704448	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142892267	chr6:13704457-13704458	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs144967167	chr6:13704462-13704463	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544616907	chr6:13704494-13704495	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138826028	chr6:13704567-13704568	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142215083	chr6:13704670-13704671	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540702249	chr6:13704680-13704681	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs547545233	chr6:13704691-13704692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535204624	chr6:13704698-13704699	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367885164	chr6:13704720-13704721	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150908031	chr6:13704733-13704734	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570448799	chr6:13704734-13704735	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs139334653	chr6:13704745-13704746	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs149613876	chr6:13704756-13704757	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562789710	chr6:13704760-13704761	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530824796	chr6:13704851-13704852	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144736205	chr6:13704869-13704870	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs79478304	chr6:13704870-13704871	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371662180	chr6:13704871-13704872	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs182192078	chr6:13704891-13704892	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368077807	chr6:13704963-13704964	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186356011	chr6:13704978-13704979	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs189870765	chr6:13705001-13705002	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546257278	chr6:13705011-13705012	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs180692832	chr6:13705013-13705014	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2013872	chr6:13705026-13705027	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559290601	chr6:13705031-13705032	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535040502	chr6:13705032-13705033	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs144360029	chr6:13705048-13705049	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs185267558	chr6:13705116-13705117	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377220533	chr6:13705134-13705135	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144334239	chr6:13705135-13705136	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs71562479	chr6:13705141-13705142	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147763708	chr6:13705163-13705164	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139471580	chr6:13705177-13705178	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs10456689	chr6:13705183-13705184	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574178329	chr6:13705194-13705195	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542795683	chr6:13705278-13705279	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538166633	chr6:13705313-13705314	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562886713	chr6:13705400-13705401	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs191361425	chr6:13705439-13705440	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536254367	chr6:13705453-13705454	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs145274797	chr6:13705501-13705502	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574959934	chr6:13705505-13705506	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs151010251	chr6:13705509-13705510	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13679000-13708400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:13681000-13708600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:13686400-13709600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:13690400-13707600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:13690600-13707600	Weak transcription	Fetal Kidney	kidney
6	chr6:13690600-13708400	Weak transcription	Aorta	Aorta
7	chr6:13691200-13708000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr6:13692000-13707600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:13692200-13708400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:13692800-13708400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:13694000-13706800	Weak transcription	Fetal Intestine Small	intestine
12	chr6:13694600-13706400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:13695000-13708000	Weak transcription	Hela-S3	cervix
14	chr6:13695000-13708200	Weak transcription	Fetal Brain Female	brain
15	chr6:13696200-13708200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:13696200-13708200	Weak transcription	Brain Substantia Nigra	brain
17	chr6:13696200-13708200	Weak transcription	Fetal Brain Male	brain
18	chr6:13696200-13708200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr6:13696400-13708000	Weak transcription	Fetal Lung	lung
20	chr6:13696600-13708400	Weak transcription	Fetal Muscle Leg	muscle
21	chr6:13697200-13705800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:13697200-13708000	Weak transcription	Brain Germinal Matrix	brain
23	chr6:13697200-13708000	Weak transcription	Fetal Intestine Large	intestine
24	chr6:13697200-13708400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:13697200-13708400	Weak transcription	NH-A	brain
26	chr6:13697800-13704400	Weak transcription	Colon Smooth Muscle	Colon
27	chr6:13698200-13708000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:13698600-13708200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr6:13698600-13708400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:13699200-13707800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr6:13699200-13708200	Weak transcription	HSMM	muscle
32	chr6:13699200-13708400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:13700400-13704600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:13700600-13708400	Weak transcription	Placenta	Placenta
35	chr6:13700800-13707800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr6:13700800-13708400	Weak transcription	Thymus	Thymus
37	chr6:13700800-13708600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr6:13700800-13710400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:13701000-13708600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr6:13701400-13708200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:13702600-13704800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:13702600-13704800	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr6:13702600-13705200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr6:13702600-13705400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr6:13702800-13706200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr6:13703000-13705000	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:13703000-13705200	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr6:13703000-13706000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr6:13703200-13704400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:13703200-13704600	Enhancers	Brain Anterior Caudate	brain

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