Variant report

Variant	nsv6327
Chromosome Location	chr8:99919634-99964563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1504)
CpG islands
(count:3302)
Chromatin interactive
region (count:72)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99953361-99953710	HepG2	liver:	n/a	n/a
2	ATF1	chr8:99939428-99939464	K562	blood:	n/a	n/a
3	ATF1	chr8:99943657-99943981	K562	blood:	n/a	n/a
4	ATF1	chr8:99922773-99923250	K562	blood:	n/a	n/a
5	ATF2	chr8:99956232-99956831	GM12878	blood:	n/a	n/a
6	ATF3	chr8:99953212-99953610	A549	lung:	n/a	n/a
7	BACH1	chr8:99960325-99960638	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:99951944-99951982	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:99956255-99957045	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:99950930-99950997	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:99960886-99961005	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:99952263-99955172	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:99957290-99957855	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:99924713-99925020	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr8:99956234-99956577	GM12878	blood:	n/a	chr8:99956446-99956456
16	BATF	chr8:99956226-99956569	GM12878	blood:	n/a	chr8:99956446-99956456
17	BATF	chr8:99934137-99934602	GM12878	blood:	n/a	chr8:99934227-99934236
18	BCL3	chr8:99956558-99957010	A549	lung:	n/a	chr8:99956564-99956573
19	BCLAF1	chr8:99956273-99957057	GM12878	blood:	n/a	chr8:99956564-99956573
20	BCLAF1	chr8:99957183-99958023	GM12878	blood:	n/a	chr8:99957199-99957208 chr8:99957412-99957425 chr8:99957418-99957431
21	BCLAF1	chr8:99953084-99953720	GM12878	blood:	n/a	chr8:99953389-99953402
22	BCLAF1	chr8:99956252-99957038	GM12878	blood:	n/a	chr8:99956564-99956573
23	BHLHE40	chr8:99953189-99953594	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:99956993-99957563	HepG2	liver:	n/a	chr8:99957412-99957428
25	BHLHE40	chr8:99952778-99953665	HepG2	liver:	n/a	n/a
26	BHLHE40	chr8:99956127-99957925	K562	blood:	n/a	chr8:99957412-99957428
27	BHLHE40	chr8:99954166-99954374	GM12878	blood:	n/a	chr8:99954293-99954309
28	BHLHE40	chr8:99963500-99963614	K562	blood:	n/a	n/a
29	BHLHE40	chr8:99939041-99939276	K562	blood:	n/a	n/a
30	BHLHE40	chr8:99958296-99958442	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:99957035-99957528	GM12878	blood:	n/a	chr8:99957412-99957428
32	BHLHE40	chr8:99956310-99956751	GM12878	blood:	n/a	n/a
33	BRCA1	chr8:99953301-99953753	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr8:99957374-99958125	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr8:99956059-99956906	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr8:99953311-99953470	HepG2	liver:	n/a	n/a
37	BRCA1	chr8:99953279-99953487	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr8:99954010-99954166	GM12878	blood:	n/a	n/a
39	BRCA1	chr8:99953133-99953155	GM12878	blood:	n/a	n/a
40	CBX3	chr8:99956187-99957034	K562	blood:	n/a	n/a
41	CBX3	chr8:99922791-99923401	K562	blood:	n/a	n/a
42	CBX3	chr8:99924532-99925244	HCT-116	colon:	n/a	n/a
43	CCNT2	chr8:99956339-99957594	K562	blood:	n/a	n/a
44	CEBPB	chr8:99925591-99925787	H1-hESC	embryonic stem cell:	n/a	chr8:99925684-99925695
45	CEBPB	chr8:99931175-99931425	MCF-7	breast:	n/a	n/a
46	CEBPB	chr8:99953829-99954308	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr8:99926695-99926844	A549	lung:	n/a	chr8:99926794-99926805 chr8:99926794-99926807
48	CEBPB	chr8:99925480-99926021	ECC-1	luminal epithelium:	n/a	chr8:99925684-99925695
49	CEBPB	chr8:99925567-99925879	HepG2	liver:	n/a	chr8:99925684-99925695
50	CEBPB	chr8:99943743-99943878	K562	blood:	n/a	n/a

(count:3302 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99960148-99960198	GM12892	blood:	n/a
2	chr8:99959723-99959773	HIPEpiC	eye:	n/a
3	chr8:99949391-99949441	HEEpiC	esophagus:	n/a
4	chr8:99960498-99960548	RPTEC	kidney:	n/a
5	chr8:99956751-99956801	MCF-7	breast:	n/a
6	chr8:99951696-99951746	Caco-2	colon:	n/a
7	chr8:99952047-99952097	U87	brain:	n/a
8	chr8:99956559-99956609	Hepatocyte	liver:	n/a
9	chr8:99960148-99960198	GM12892	blood:	n/a
10	chr8:99959723-99959773	HIPEpiC	eye:	n/a
11	chr8:99949391-99949441	HEEpiC	esophagus:	n/a
12	chr8:99960498-99960548	RPTEC	kidney:	n/a
13	chr8:99956751-99956801	MCF-7	breast:	n/a
14	chr8:99951696-99951746	Caco-2	colon:	n/a
15	chr8:99952047-99952097	U87	brain:	n/a
16	chr8:99956559-99956609	Hepatocyte	liver:	n/a
17	chr8:99950917-99950967	PFSK-1	brain:	n/a
18	chr8:99961376-99961426	AG09309	skin:	n/a
19	chr8:99960500-99960550	AG04450	lung:	fetal
20	chr8:99962118-99962168	ProgFib	skin:	n/a
21	chr8:99960498-99960548	HMEC	breast:	n/a
22	chr8:99956559-99956609	HAEpiC	amniotic membrane:	n/a
23	chr8:99959723-99959773	ProgFib	skin:	n/a
24	chr8:99955563-99955613	HCT-116	colon:	n/a
25	chr8:99962013-99962063	HAEpiC	amniotic membrane:	n/a
26	chr8:99962013-99962063	HepG2	liver:	n/a
27	chr8:99955563-99955613	HL-60	blood:	n/a
28	chr8:99957225-99957275	HL-60	blood:	n/a
29	chr8:99962013-99962063	HL-60	blood:	n/a
30	chr8:99962013-99962063	MCF-7	breast:	n/a
31	chr8:99956874-99956924	HNPCEpiC	eye:	n/a
32	chr8:99960498-99960548	ProgFib	skin:	n/a
33	chr8:99953809-99953859	ovcar-3	ovarian:	n/a
34	chr8:99956574-99956624	U87	brain:	n/a
35	chr8:99962118-99962168	HL-60	blood:	n/a
36	chr8:99951696-99951746	NB4	blood:	n/a
37	chr8:99962013-99962063	HEK293	kidney:	embryo
38	chr8:99960843-99960893	GM19239	blood:	n/a
39	chr8:99961122-99961172	GM12892	blood:	n/a
40	chr8:99955989-99956039	LNCaP	prostate:	n/a
41	chr8:99955563-99955613	HAEpiC	amniotic membrane:	n/a
42	chr8:99951730-99951780	GM06990	blood:	n/a
43	chr8:99962347-99962397	PrEC	prostate:	n/a
44	chr8:99956467-99956517	A549	lung:	n/a
45	chr8:99953947-99953997	HRE	kidney:	n/a
46	chr8:99959602-99959652	T-47D	breast:	n/a
47	chr8:99954432-99954482	AG10803	skin:	n/a
48	chr8:99952217-99952267	A549	lung:	n/a
49	chr8:99959602-99959652	HCF	heart:	n/a
50	chr8:99957225-99957275	AG09319	gingival:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:99836481..99839453-chr8:99955374..99958557,4	MCF-7	breast:
2	chr8:99952913..99953621-chr8:100370794..100371379,2	MCF-7	breast:
3	chr8:99947363..99950465-chr8:99951087..99953712,3	K562	blood:
4	chr8:99959441..99961550-chr8:99971989..99973976,2	K562	blood:
5	chr8:99947363..99950465-chr8:99951087..99953712,3	K562	blood:
6	chr8:99930162..99932439-chr8:100009784..100012613,2	K562	blood:
7	chr8:99836684..99839127-chr8:99955180..99958109,2	K562	blood:
8	chr8:99949280..99952600-chr8:100024277..100026465,3	MCF-7	breast:
9	chr8:99941131..99944332-chr8:99944576..99947725,3	K562	blood:
10	chr8:99952140..99962153-chr8:100006475..100015090,25	MCF-7	breast:
11	chr8:99931677..99933733-chr8:99937087..99939527,3	MCF-7	breast:
12	chr8:99912065..99913675-chr8:99919981..99921782,2	K562	blood:
13	chr8:99936963..99939745-chr8:99942656..99945387,2	MCF-7	breast:
14	chr8:99936963..99939745-chr8:99942656..99945387,2	MCF-7	breast:
15	chr8:99960776..99964235-chr8:99964310..99968254,5	K562	blood:
16	chr8:99942235..99943803-chr8:99945712..99947725,2	K562	blood:
17	chr8:99953182..99954172-chr8:100024751..100025376,2	MCF-7	breast:
18	chr8:99953586..99962238-chr8:100023509..100028680,26	MCF-7	breast:
19	chr8:99954936..99956657-chr8:100904324..100906629,2	MCF-7	breast:
20	chr8:99900255..99902088-chr8:99919103..99920638,2	MCF-7	breast:
21	chr8:99931553..99934461-chr8:99944325..99946823,2	MCF-7	breast:
22	chr8:99941131..99944332-chr8:99944576..99947725,3	K562	blood:
23	chr8:99914410..99918867-chr8:99920230..99924204,4	K562	blood:
24	chr8:99942466..99945481-chr8:99954331..99957519,4	K562	blood:
25	chr8:99931677..99933733-chr8:99937087..99939527,3	MCF-7	breast:
26	chr8:99935777..99938346-chr8:99942242..99944176,3	K562	blood:
27	chr8:99836898..99839856-chr8:99963971..99965624,2	K562	blood:
28	chr8:99964252..99966277-chr8:100025241..100027364,3	MCF-7	breast:
29	chr8:99717523..99718404-chr8:99953348..99953880,2	MCF-7	breast:
30	chr8:99951388..99953620-chr8:100021426..100022985,2	K562	blood:
31	chr8:99835536..99838329-chr8:99956256..99958052,2	MCF-7	breast:
32	chr8:99914629..99917036-chr8:99927739..99929359,2	MCF-7	breast:
33	chr8:99949821..99952393-chr8:99958605..99960379,2	K562	blood:
34	chr8:99836199..99839281-chr8:99955647..99960130,4	K562	blood:
35	chr8:99949821..99952393-chr8:99958605..99960379,2	K562	blood:
36	chr8:99923112..99924735-chr8:99939317..99940986,2	MCF-7	breast:
37	chr8:99714532..99716117-chr8:99964323..99966058,2	MCF-7	breast:
38	chr8:99910044..99913955-chr8:99926484..99929413,3	K562	blood:
39	chr8:99952762..99963438-chr8:100019139..100031293,37	MCF-7	breast:
40	chr8:99952714..99953511-chr8:101138115..101138641,2	MCF-7	breast:
41	chr12:120635323..120636844-chr8:99936568..99939142,2	MCF-7	breast:
42	chr8:99661906..99664329-chr8:99956094..99958895,2	MCF-7	breast:
43	chr8:99962836..99965114-chr8:99973570..99976399,2	K562	blood:
44	chr8:99962872..99965221-chr8:99992608..99995397,2	MCF-7	breast:
45	chr8:99956762..99958304-chr8:100013613..100016438,2	K562	blood:
46	chr8:99946409..99949543-chr8:99954979..99957552,3	K562	blood:
47	chr8:99956335..99957904-chr8:100286239..100289117,2	MCF-7	breast:
48	chr8:99901798..99904036-chr8:99961157..99963131,2	K562	blood:
49	chr8:99941648..99943992-chr8:99953695..99958412,4	MCF-7	breast:
50	chr1:116960076..116962141-chr8:99963781..99966364,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL2-7	chr8:99933461-99933778	NONHSAT127937
2	lnc-OSR2-3	chr8:99956631-99957051	NONHSAT127938
3	lnc-NIPAL2-5	chr8:99954606-99954873	NONHSAT127935
4	lnc-OSR2-3	chr8:99958259-99958530	NONHSAT127938
5	lnc-OSR2-4	chr8:99955823-99956326	ENSG00000271930.1

No data

Variant related genes	Relation type
STK3	TF binding region
MRP63P7	TF binding region
RN7SKP85	TF binding region
OSR2	TF binding region
ENSG00000253415	TF binding region
ENSG00000271930	TF binding region
STK3	CpG island
MRP63P7	CpG island
RN7SKP85	CpG island
OSR2	CpG island
ENSG00000253415	CpG island
ENSG00000271930	CpG island
ENSG00000271930	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253415	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000263842	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000223281	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000203865	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000164919	chromatin interactions
ENSG00000229625	chromatin interactions
ENSG00000254312	chromatin interactions

Extended variants
information (count: 1510 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1510 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577947809	chr8:99919634-99919635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377262280	chr8:99919636-99919637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540230581	chr8:99919644-99919645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553790187	chr8:99919654-99919655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573708401	chr8:99919672-99919673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543061357	chr8:99919681-99919682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562863196	chr8:99919716-99919717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560746106	chr8:99919720-99919721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544909347	chr8:99919731-99919732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192154855	chr8:99919789-99919790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527629798	chr8:99919800-99919801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375316001	chr8:99919894-99919895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547404503	chr8:99919895-99919896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574637901	chr8:99919926-99919927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138514614	chr8:99919935-99919936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529715106	chr8:99920080-99920081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184551181	chr8:99920091-99920092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149637610	chr8:99920092-99920093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189335844	chr8:99920149-99920150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558118119	chr8:99920189-99920190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546808653	chr8:99920243-99920244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs180818740	chr8:99920247-99920248	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs143357521	chr8:99920354-99920355	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184635264	chr8:99920364-99920365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533831585	chr8:99920381-99920382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542671104	chr8:99920402-99920403	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369930425	chr8:99920590-99920591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs111675450	chr8:99920668-99920669	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576488625	chr8:99920685-99920686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537139572	chr8:99920732-99920733	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545184788	chr8:99920737-99920738	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565113513	chr8:99920767-99920768	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112486796	chr8:99920800-99920801	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145960838	chr8:99920840-99920841	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561187191	chr8:99920849-99920850	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs374846274	chr8:99920851-99920852	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs557359782	chr8:99920864-99920865	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577146073	chr8:99920902-99920903	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565026794	chr8:99920932-99920933	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs529679828	chr8:99920969-99920970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554024323	chr8:99920983-99920984	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569732530	chr8:99921002-99921003	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs79633577	chr8:99921019-99921020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs113951313	chr8:99921026-99921027	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181505105	chr8:99921086-99921087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186435732	chr8:99921087-99921088	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111827268	chr8:99921088-99921089	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs567651480	chr8:99921089-99921090	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200104367	chr8:99921093-99921094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs141490802	chr8:99921104-99921105	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	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
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99912000-99920800	Weak transcription	Ovary	ovary
2	chr8:99914400-99923000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:99914400-99924600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:99918800-99923000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:99918800-99924400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:99918800-99926400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:99922600-99923400	Enhancers	Dnd41	blood
8	chr8:99922600-99923400	Enhancers	NHEK	skin
9	chr8:99922800-99923200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:99922800-99923200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:99922800-99923200	Enhancers	GM12878-XiMat	blood
12	chr8:99922800-99923400	Enhancers	HMEC	breast
13	chr8:99922800-99923400	Enhancers	K562	blood
14	chr8:99922800-99925400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr8:99923000-99923200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:99923000-99923400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:99923000-99923400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:99923000-99923400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr8:99923000-99923600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:99923200-99923400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:99923200-99924600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:99923200-99924800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:99923400-99924400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:99923400-99924400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:99923400-99924600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:99923400-99924600	Weak transcription	HMEC	breast
27	chr8:99923400-99924600	Weak transcription	NHEK	skin
28	chr8:99923400-99925000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:99923600-99924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr8:99923600-99924600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr8:99924200-99924600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr8:99924200-99924800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:99924200-99925000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:99924400-99924600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:99924400-99925000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:99924400-99925000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:99924400-99927200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:99924600-99924800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr8:99924600-99924800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:99924600-99924800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr8:99924600-99925000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:99924600-99925000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:99924600-99925000	Enhancers	NHEK	skin
44	chr8:99924600-99925200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr8:99924600-99925400	Enhancers	HMEC	breast
46	chr8:99924600-99925800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr8:99924600-99925800	Enhancers	A549	lung
48	chr8:99924800-99925000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:99924800-99925000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:99924800-99925200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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