Variant report

Variant	nsv890975
Chromosome Location	chr8:67983796-68032058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:122)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:68022007-68022483	K562	blood:	n/a	n/a
2	ARID3A	chr8:68026510-68027171	K562	blood:	n/a	n/a
3	ARID3A	chr8:68009478-68009999	K562	blood:	n/a	n/a
4	ATF1	chr8:68022028-68022347	K562	blood:	n/a	n/a
5	BACH1	chr8:68013863-68013960	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:67998010-67998079	K562	blood:	n/a	n/a
7	BHLHE40	chr8:68021797-68022409	K562	blood:	n/a	n/a
8	CBX3	chr8:68021929-68022308	K562	blood:	n/a	n/a
9	CBX3	chr8:68021765-68022411	K562	blood:	n/a	n/a
10	CCNT2	chr8:68021959-68022495	K562	blood:	n/a	n/a
11	CCNT2	chr8:68026748-68027196	K562	blood:	n/a	n/a
12	CEBPB	chr8:68007657-68007868	HepG2	liver:	n/a	chr8:68007705-68007716
13	CEBPB	chr8:67996446-67996798	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:68021700-68022376	K562	blood:	n/a	n/a
15	CEBPB	chr8:68021723-68021959	K562	blood:	n/a	n/a
16	CEBPB	chr8:68007700-68007715	K562	blood:	n/a	n/a
17	CEBPB	chr8:68022022-68022340	K562	blood:	n/a	n/a
18	CEBPB	chr8:68003361-68003523	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:68007624-68007824	A549	lung:	n/a	chr8:68007705-68007716
20	CEBPB	chr8:68021686-68022377	K562	blood:	n/a	n/a
21	CEBPD	chr8:68026644-68027103	K562	blood:	n/a	n/a
22	CEBPD	chr8:68026684-68027035	K562	blood:	n/a	n/a
23	CEBPD	chr8:68021821-68022549	K562	blood:	n/a	n/a
24	CEBPD	chr8:68021932-68022528	K562	blood:	n/a	n/a
25	CHD2	chr8:68022182-68022373	K562	blood:	n/a	n/a
26	CTCF	chr8:68021280-68021430	HL-60	blood:	n/a	n/a
27	CTCF	chr8:67984249-67984271	GM10248	blood:	n/a	n/a
28	CTCF	chr8:68017310-68017375	GM20000	blood:	n/a	n/a
29	CTCF	chr8:67987860-67988010	NHEK	skin:	n/a	n/a
30	CTCF	chr8:68022108-68022189	K562	blood:	n/a	n/a
31	CTCF	chr8:68000542-68000640	Lung_OC	lung:	n/a	n/a
32	CUX1	chr8:67985091-67985145	K562	blood:	n/a	n/a
33	CUX1	chr8:68014271-68014273	K562	blood:	n/a	n/a
34	CUX1	chr8:68022037-68022364	K562	blood:	n/a	n/a
35	E2F4	chr8:68014335-68014520	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr8:67991769-67991800	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:68026994-68027180	MCF10A-Er-Src	breast:	n/a	n/a
38	EGR1	chr8:68022001-68022504	K562	blood:	n/a	n/a
39	EGR1	chr8:68022051-68022447	K562	blood:	n/a	n/a
40	EP300	chr8:68021873-68022570	K562	blood:	n/a	n/a
41	EP300	chr8:68021957-68022528	HepG2	liver:	n/a	n/a
42	EP300	chr8:68022025-68022508	HepG2	liver:	n/a	n/a
43	EP300	chr8:68026699-68027211	K562	blood:	n/a	chr8:68026841-68026855 chr8:68026918-68026932
44	EP300	chr8:68022052-68022400	K562	blood:	n/a	n/a
45	FAM48A	chr8:68027320-68027339	GM12878	blood:	n/a	n/a
46	FOS	chr8:67985241-67985373	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:67985209-67985433	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr8:68022009-68022653	HepG2	liver:	n/a	n/a
49	FOXA1	chr8:68021953-68022606	HepG2	liver:	n/a	n/a
50	FOXA1	chr8:67985128-67985517	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67996256-67996306	HEK293	kidney:	embryo
2	chr8:67996256-67996306	HCF	heart:	n/a
3	chr8:67996256-67996306	SK-N-SH_RA	brain:	n/a
4	chr8:68022262-68022312	PFSK-1	brain:	n/a
5	chr8:68022262-68022312	NB4	blood:	n/a
6	chr8:68022262-68022312	HRCEpiC	kidney:	n/a
7	chr8:68022262-68022312	NT2-D1	testis:	n/a
8	chr8:67996256-67996306	BJ	skin:	n/a
9	chr8:67996256-67996306	AoSMC	blood vessel:	n/a
10	chr8:68022262-68022312	HCM	heart:	n/a
11	chr8:68022262-68022312	BJ	skin:	n/a
12	chr8:68022262-68022312	Hela-S3	cervix:	n/a
13	chr8:67996256-67996306	SAEC	small airway:	n/a
14	chr8:68022262-68022312	CMK	blood:	n/a
15	chr8:68022262-68022312	HepG2	liver:	n/a
16	chr8:68022262-68022312	U87	brain:	n/a
17	chr8:68022262-68022312	Caco-2	colon:	n/a
18	chr8:68022262-68022312	LNCaP	prostate:	n/a
19	chr8:67996256-67996306	HAEpiC	amniotic membrane:	n/a
20	chr8:67996256-67996306	HRCEpiC	kidney:	n/a
21	chr8:68022262-68022312	AG09309	skin:	n/a
22	chr8:67996256-67996306	NHDF-neo	bronchial:	n/a
23	chr8:68022262-68022312	ProgFib	skin:	n/a
24	chr8:68022262-68022312	HCF	heart:	n/a
25	chr8:68022262-68022312	SK-N-SH_RA	brain:	n/a
26	chr8:68022262-68022312	AG09319	gingival:	n/a
27	chr8:68022262-68022312	SK-N-MC	brain:	n/a
28	chr8:67996256-67996306	BE2_C	brain:	n/a
29	chr8:67996256-67996306	HCT-116	colon:	n/a
30	chr8:68022262-68022312	BE2_C	brain:	n/a
31	chr8:68022262-68022312	HMEC	breast:	n/a
32	chr8:68022262-68022312	HEEpiC	esophagus:	n/a
33	chr8:67996256-67996306	SK-N-SH	brain:	n/a
34	chr8:67996256-67996306	AG04450	lung:	fetal
35	chr8:68022262-68022312	SKMC	muscle:	n/a
36	chr8:68022262-68022312	HL-60	blood:	n/a
37	chr8:68022262-68022312	GM12892	blood:	n/a
38	chr8:67996256-67996306	AG09309	skin:	n/a
39	chr8:67996256-67996306	HepG2	liver:	n/a
40	chr8:67996256-67996306	HRE	kidney:	n/a
41	chr8:67996256-67996306	IMR90	lung:	fetal
42	chr8:67996256-67996306	GM19239	blood:	n/a
43	chr8:68022262-68022312	AG04449	skin:	fetal
44	chr8:67996256-67996306	SKMC	muscle:	n/a
45	chr8:67996256-67996306	ProgFib	skin:	n/a
46	chr8:67996256-67996306	HMEC	breast:	n/a
47	chr8:67996256-67996306	RPTEC	kidney:	n/a
48	chr8:68022262-68022312	ovcar-3	ovarian:	n/a
49	chr8:68022262-68022312	HEK293	kidney:	embryo
50	chr8:67996256-67996306	GM06990	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67974200..67976487-chr8:67991987..67993603,2	K562	blood:
2	chr8:67977500..67979616-chr8:68012864..68015307,2	MCF-7	breast:
3	chr8:67831901..67834274-chr8:68007659..68009308,2	K562	blood:
4	chr8:67981900..67985386-chr8:67987036..67990372,4	K562	blood:
5	chr8:67973427..67978093-chr8:68011189..68018690,8	K562	blood:
6	chr8:67830248..67833464-chr8:68001607..68004691,3	K562	blood:
7	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
8	chr8:67990308..67993966-chr8:67998315..68001185,4	K562	blood:
9	chr8:67969000..67971915-chr8:68028216..68029773,2	K562	blood:
10	chr8:67996527..67998674-chr8:68001336..68003420,2	K562	blood:
11	chr8:67977046..67978803-chr8:67992749..67996349,3	K562	blood:
12	chr8:67985384..67988219-chr8:68025028..68027428,3	K562	blood:
13	chr8:67976675..67980176-chr8:67982253..67985496,4	MCF-7	breast:
14	chr8:67990308..67993966-chr8:67998315..68001185,4	K562	blood:
15	chr8:67972943..67975596-chr8:68018499..68020394,2	MCF-7	breast:
16	chr8:68019313..68021388-chr8:68023240..68024925,2	K562	blood:
17	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
18	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
19	chr8:67983356..67985019-chr8:67992324..67994930,2	MCF-7	breast:
20	chr8:67983356..67985019-chr8:67992324..67994930,2	MCF-7	breast:
21	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
22	chr8:68021467..68023804-chr8:68064580..68067516,2	K562	blood:
23	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
24	chr8:67973913..67977272-chr8:68024656..68026462,3	K562	blood:
25	chr8:67973320..67975625-chr8:67995468..67997290,2	K562	blood:
26	chr8:67981584..67984987-chr8:67987255..67990503,3	MCF-7	breast:
27	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
28	chr8:67341475..67343466-chr8:67983783..67985508,2	MCF-7	breast:
29	chr8:67976406..67978604-chr8:68001660..68003649,2	K562	blood:
30	chr8:67981584..67984987-chr8:67987255..67990503,3	MCF-7	breast:
31	chr8:67831270..67834163-chr8:68004872..68007019,2	K562	blood:
32	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
33	chr8:68030814..68032510-chr8:68038981..68041972,2	K562	blood:
34	chr8:67996527..67998674-chr8:68001336..68003420,2	K562	blood:
35	chr8:67990677..67996100-chr8:67997550..68001970,5	K562	blood:
36	chr8:67981623..67983543-chr8:67991584..67993705,2	K562	blood:
37	chr8:67981900..67985386-chr8:67987036..67990372,4	K562	blood:
38	chr8:67985384..67988219-chr8:68025028..68027428,3	K562	blood:
39	chr8:67978540..67980056-chr8:67997064..67998672,2	K562	blood:
40	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
41	chr8:68006861..68009461-chr8:68010974..68012762,2	K562	blood:
42	chr8:67975625..67978171-chr8:68007327..68009716,2	MCF-7	breast:
43	chr8:67976148..67978802-chr8:68002770..68006546,3	K562	blood:
44	chr8:68019313..68021388-chr8:68023240..68024925,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COPS5-1	chr8:67997226-67997654	expReg_chr8_3344_-

No data

Variant related genes	Relation type
CSPP1	TF binding region
RNA5SP268	TF binding region
COPS5	TF binding region
CSPP1	CpG island
RNA5SP268	CpG island
COPS5	CpG island
ENSG00000121022	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000252637	chromatin interactions
ENSG00000266491	chromatin interactions
ENSG00000147576	chromatin interactions

Extended variants
information (count: 1521 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1521 , 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	rs11985037	chr8:67983796-67983797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534587740	chr8:67983828-67983829	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139908079	chr8:67983841-67983842	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567884268	chr8:67983885-67983886	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537255869	chr8:67984086-67984087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs557137374	chr8:67984100-67984101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201929318	chr8:67984107-67984108	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557424335	chr8:67984108-67984109	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577260755	chr8:67984136-67984137	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183449978	chr8:67984157-67984158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143321850	chr8:67984167-67984168	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572876559	chr8:67984221-67984222	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs573308456	chr8:67984226-67984227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375220864	chr8:67984243-67984244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562389908	chr8:67984290-67984291	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368110264	chr8:67984296-67984297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371317821	chr8:67984311-67984312	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374828131	chr8:67984312-67984313	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs187016873	chr8:67984340-67984341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs191887213	chr8:67984356-67984357	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs113321741	chr8:67984420-67984421	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575707043	chr8:67984433-67984434	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183421857	chr8:67984444-67984445	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112959621	chr8:67984501-67984502	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs564571080	chr8:67984502-67984503	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575107749	chr8:67984522-67984523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78162470	chr8:67984523-67984524	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs34242021	chr8:67984556-67984557	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550421392	chr8:67984660-67984661	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115902331	chr8:67984740-67984741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11986053	chr8:67984742-67984743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564043137	chr8:67984839-67984840	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564669063	chr8:67984843-67984844	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs80004385	chr8:67984875-67984876	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376341420	chr8:67984896-67984897	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540876122	chr8:67985039-67985040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs117270829	chr8:67985049-67985050	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550751530	chr8:67985089-67985090	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188423797	chr8:67985090-67985091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377753829	chr8:67985104-67985105	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539925119	chr8:67985116-67985117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs115012780	chr8:67985118-67985119	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566844741	chr8:67985121-67985122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115256088	chr8:67985122-67985123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs58087584	chr8:67985125-67985126	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78697552	chr8:67985126-67985127	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs12542173	chr8:67985208-67985209	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555836833	chr8:67985230-67985231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs12542194	chr8:67985333-67985334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544606779	chr8:67985361-67985362	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	16751803	CNVD
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	17142309	CNVD
Glioblastoma multiforme	19115005	CNVD
Breast cancer	22522925	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	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	chr8:67977600-67989400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:67977600-67989600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:67977600-67998200	Weak transcription	Gastric	stomach
4	chr8:67977800-67986600	Weak transcription	Fetal Intestine Large	intestine
5	chr8:67977800-67986800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr8:67977800-67987200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:67977800-67987400	Weak transcription	Primary B cells from cord blood	blood
8	chr8:67977800-67987400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr8:67977800-68009200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:67977800-68010000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr8:67977800-68013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:67977800-68021800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:67977800-68044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr8:67978000-67986400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:67978000-67987000	Weak transcription	Fetal Stomach	stomach
16	chr8:67978000-67987200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr8:67978000-67987200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr8:67978000-67987400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr8:67978000-67987600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr8:67978000-67989400	Weak transcription	Small Intestine	intestine
21	chr8:67978000-67995400	Weak transcription	Colonic Mucosa	Colon
22	chr8:67978000-67996800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:67978000-68012200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:67978200-67983800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr8:67978200-67987000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr8:67978200-67987000	Weak transcription	Left Ventricle	heart
27	chr8:67978200-67987200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:67978200-67987200	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr8:67978200-67987200	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr8:67978200-67987200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:67978200-67987200	Weak transcription	Liver	Liver
32	chr8:67978200-67987200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr8:67978200-67987400	Weak transcription	Adipose Nuclei	Adipose
34	chr8:67978200-67987400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr8:67978200-67987400	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr8:67978200-67987800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr8:67978200-67987800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr8:67978200-67987800	Weak transcription	Lung	lung
39	chr8:67978200-67989000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr8:67978200-67990600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:67978200-67992000	Weak transcription	Aorta	Aorta
42	chr8:67978200-67992600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:67978200-68006000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr8:67978200-68012600	Weak transcription	HUVEC	blood vessel
45	chr8:67978200-68074400	Weak transcription	Esophagus	oesophagus
46	chr8:67978400-67985800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:67978400-67986400	Weak transcription	NH-A	brain
48	chr8:67978400-67986600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr8:67978400-67987200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr8:67978400-67987400	Weak transcription	Primary hematopoietic stem cells	blood

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