Variant report

Variant	nsv1033345
Chromosome Location	chr8:95556375-95570533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:837)
CpG islands
(count:916)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:95569910-95569916	K562	blood:	n/a	n/a
2	ARID3A	chr8:95561953-95561992	K562	blood:	n/a	n/a
3	ARID3A	chr8:95565426-95566634	HepG2	liver:	n/a	n/a
4	ATF1	chr8:95561825-95562110	K562	blood:	n/a	n/a
5	ATF1	chr8:95569899-95570225	K562	blood:	n/a	n/a
6	ATF1	chr8:95565579-95566141	K562	blood:	n/a	n/a
7	ATF2	chr8:95565566-95566121	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:95565522-95566225	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:95565524-95566160	GM12878	blood:	n/a	n/a
10	ATF2	chr8:95565395-95566440	GM12878	blood:	n/a	n/a
11	ATF3	chr8:95565322-95566218	A549	lung:	n/a	n/a
12	ATF3	chr8:95565622-95565918	K562	blood:	n/a	n/a
13	ATF3	chr8:95565427-95566185	A549	lung:	n/a	n/a
14	BACH1	chr8:95559244-95559249	K562	blood:	n/a	n/a
15	BACH1	chr8:95565507-95566395	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr8:95565367-95566295	A549	lung:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
17	BCL3	chr8:95565360-95566282	A549	lung:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
18	BCLAF1	chr8:95565466-95566185	GM12878	blood:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
19	BCLAF1	chr8:95565527-95566107	K562	blood:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
20	BCLAF1	chr8:95565349-95566233	GM12878	blood:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
21	BHLHE40	chr8:95565477-95566450	HepG2	liver:	n/a	n/a
22	BHLHE40	chr8:95565323-95566674	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:95565474-95566799	K562	blood:	n/a	n/a
24	BRCA1	chr8:95565594-95566030	HepG2	liver:	n/a	n/a
25	BRCA1	chr8:95564895-95565001	HepG2	liver:	n/a	n/a
26	BRCA1	chr8:95565462-95566279	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr8:95565670-95566434	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr8:95565523-95566102	K562	blood:	n/a	n/a
29	CBX3	chr8:95569680-95570225	K562	blood:	n/a	n/a
30	CBX3	chr8:95565300-95566413	K562	blood:	n/a	n/a
31	CCNT2	chr8:95565589-95566065	K562	blood:	n/a	n/a
32	CEBPB	chr8:95565701-95566473	K562	blood:	n/a	n/a
33	CEBPB	chr8:95565550-95566466	A549	lung:	n/a	n/a
34	CEBPB	chr8:95565702-95566387	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:95565519-95566425	A549	lung:	n/a	n/a
36	CEBPB	chr8:95565531-95566094	K562	blood:	n/a	n/a
37	CEBPB	chr8:95565764-95566115	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:95565353-95566299	GM12878	blood:	n/a	n/a
39	CEBPB	chr8:95565523-95566485	Hela-S3	cervix:	n/a	n/a
40	CEBPD	chr8:95565434-95566560	K562	blood:	n/a	n/a
41	CEBPD	chr8:95565564-95566054	HepG2	liver:	n/a	n/a
42	CEBPD	chr8:95565448-95566126	HepG2	liver:	n/a	n/a
43	CEBPD	chr8:95565488-95566133	K562	blood:	n/a	n/a
44	CHD1	chr8:95566496-95566694	GM12878	blood:	n/a	n/a
45	CHD1	chr8:95566013-95566310	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr8:95565345-95566250	GM12878	blood:	n/a	n/a
47	CHD2	chr8:95565304-95566462	HepG2	liver:	n/a	n/a
48	CHD2	chr8:95565549-95566324	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:95565608-95566178	K562	blood:	n/a	n/a
50	CHD2	chr8:95565311-95566352	Hela-S3	cervix:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95566380-95566430	NT2-D1	testis:	n/a
2	chr8:95566380-95566430	NT2-D1	testis:	n/a
3	chr8:95565249-95565299	NH-A	brain:	n/a
4	chr8:95565953-95566003	PrEC	prostate:	n/a
5	chr8:95565249-95565299	RPTEC	kidney:	n/a
6	chr8:95566380-95566430	HCF	heart:	n/a
7	chr8:95565789-95565839	HCF	heart:	n/a
8	chr8:95565249-95565299	Hela-S3	cervix:	n/a
9	chr8:95566476-95566526	GM12892	blood:	n/a
10	chr8:95566670-95566720	GM06990	blood:	n/a
11	chr8:95566380-95566430	IMR90	lung:	fetal
12	chr8:95565953-95566003	AoSMC	blood vessel:	n/a
13	chr8:95565682-95565732	Jurkat	blood:	n/a
14	chr8:95566380-95566430	U87	brain:	n/a
15	chr8:95569815-95569865	RPTEC	kidney:	n/a
16	chr8:95565249-95565299	GM19239	blood:	n/a
17	chr8:95565789-95565839	HL-60	blood:	n/a
18	chr8:95565801-95565851	NT2-D1	testis:	n/a
19	chr8:95563352-95563402	MCF10A-Er-Src	breast:	n/a
20	chr8:95569815-95569865	GM06990	blood:	n/a
21	chr8:95563352-95563402	CMK	blood:	n/a
22	chr8:95565249-95565299	BJ	skin:	n/a
23	chr8:95565953-95566003	Jurkat	blood:	n/a
24	chr8:95569815-95569865	GM12891	blood:	n/a
25	chr8:95566223-95566273	HNPCEpiC	eye:	n/a
26	chr8:95565801-95565851	HCF	heart:	n/a
27	chr8:95565392-95565442	HEK293	kidney:	embryo
28	chr8:95565392-95565442	HNPCEpiC	eye:	n/a
29	chr8:95565739-95565789	RPTEC	kidney:	n/a
30	chr8:95565249-95565299	HCF	heart:	n/a
31	chr8:95565682-95565732	U87	brain:	n/a
32	chr8:95566670-95566720	RPTEC	kidney:	n/a
33	chr8:95564335-95564385	LNCaP	prostate:	n/a
34	chr8:95566223-95566273	Hepatocyte	liver:	n/a
35	chr8:95565682-95565732	AG09319	gingival:	n/a
36	chr8:95566476-95566526	HCF	heart:	n/a
37	chr8:95569815-95569865	IMR90	lung:	fetal
38	chr8:95566223-95566273	SK-N-SH	brain:	n/a
39	chr8:95566670-95566720	Jurkat	blood:	n/a
40	chr8:95565801-95565851	HEK293	kidney:	embryo
41	chr8:95565682-95565732	NHDF-neo	bronchial:	n/a
42	chr8:95565249-95565299	HRCEpiC	kidney:	n/a
43	chr8:95565502-95565552	CMK	blood:	n/a
44	chr8:95565682-95565732	HCPEpiC	choroid plexus:	n/a
45	chr8:95565682-95565732	BE2_C	brain:	n/a
46	chr8:95566223-95566273	HRE	kidney:	n/a
47	chr8:95565682-95565732	A549	lung:	n/a
48	chr8:95565801-95565851	HCPEpiC	choroid plexus:	n/a
49	chr8:95564335-95564385	Caco-2	colon:	n/a
50	chr8:95565789-95565839	K562	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95563755..95566398-chr8:95651251..95655119,6	MCF-7	breast:
2	chr8:95548641..95550186-chr8:95556999..95558731,2	K562	blood:
3	chr8:95555945..95557652-chr8:95557953..95559866,2	MCF-7	breast:
4	chr8:95567263..95568889-chr8:95730604..95733180,2	K562	blood:
5	chr8:95555945..95557652-chr8:95557953..95559866,2	MCF-7	breast:
6	chr8:95567356..95569576-chr8:95586722..95588643,2	MCF-7	breast:
7	chr8:95565950..95567882-chr8:95569895..95571408,2	MCF-7	breast:
8	chr8:95557664..95559966-chr8:95650412..95652511,2	MCF-7	breast:
9	chr8:95554974..95557880-chr8:95564950..95566849,3	MCF-7	breast:
10	chr8:95429301..95430964-chr8:95556337..95558310,2	MCF-7	breast:
11	chr8:95564818..95567463-chr8:95729750..95733556,7	MCF-7	breast:
12	chr8:95554974..95557880-chr8:95564950..95566849,3	MCF-7	breast:
13	chr8:95568828..95570983-chr8:95731754..95733719,2	MCF-7	breast:
14	chr8:95564633..95567300-chr8:95651331..95653603,2	MCF-7	breast:
15	chr8:95564422..95566417-chr8:95731300..95733624,2	K562	blood:
16	chr8:95537067..95539960-chr8:95561344..95563037,2	MCF-7	breast:
17	chr8:95564312..95566828-chr8:95731001..95732970,2	MCF-7	breast:
18	chr8:95558228..95561115-chr8:95906355..95909204,2	K562	blood:
19	chr8:95556183..95559262-chr8:95651441..95653267,3	MCF-7	breast:
20	chr8:95569874..95571629-chr8:95571639..95574216,2	K562	blood:
21	chr8:95564422..95566417-chr8:95730460..95733624,3	K562	blood:
22	chr8:95564914..95567104-chr8:95570346..95572285,2	K562	blood:
23	chr8:95565366..95567177-chr8:96036825..96038672,2	K562	blood:
24	chr8:95553642..95556255-chr8:95557800..95559824,2	K562	blood:
25	chr12:39298720..39299544-chr8:95565528..95566062,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC023632.1-2	chr8:95565982-95566135	NONHSAT127779
2	lnc-AC023632.1-2	chr8:95565982-95566135	NONHSAT127777
3	lnc-KIAA1429-2	chr8:95566810-95567299	NONHSAT127780
4	lnc-AC023632.1-2	chr8:95565982-95566135	NONHSAT127778

No data

Variant related genes	Relation type
ENSG00000212997	TF binding region
ENSG00000253704	TF binding region
KIAA1429	TF binding region
ENSG00000212997	CpG island
ENSG00000253704	CpG island
KIAA1429	CpG island
ENSG00000261437	chromatin interactions
ENSG00000139117	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000156162	chromatin interactions
ENSG00000253704	chromatin interactions
ENSG00000104413	chromatin interactions
ENSG00000164944	chromatin interactions
ENSG00000175305	chromatin interactions
ENSG00000212997	chromatin interactions

Extended variants
information (count: 561 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570424303	chr8:95556380-95556381	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs181543149	chr8:95556422-95556423	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs370622595	chr8:95556425-95556426	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs546858870	chr8:95556479-95556480	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs566400399	chr8:95556513-95556514	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs535364298	chr8:95556567-95556568	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs555102191	chr8:95556589-95556590	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs112148681	chr8:95556618-95556619	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs186197501	chr8:95556623-95556624	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs557996430	chr8:95556695-95556696	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs112797011	chr8:95556703-95556704	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs138400316	chr8:95556704-95556705	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs560496772	chr8:95556705-95556706	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs191404667	chr8:95556716-95556717	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs543354925	chr8:95556783-95556784	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs563065976	chr8:95556799-95556800	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs181432409	chr8:95556805-95556806	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs551224168	chr8:95556831-95556832	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs564062490	chr8:95556843-95556844	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs561987510	chr8:95556857-95556858	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs397892475	chr8:95556891-95556892	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs397891330	chr8:95556892-95556893	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs75924812	chr8:95556894-95556895	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs533064099	chr8:95556904-95556905	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs547770348	chr8:95556908-95556909	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs370776348	chr8:95556909-95556910	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs546139995	chr8:95556936-95556937	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs141931615	chr8:95556945-95556946	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs544587277	chr8:95556958-95556959	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs3099419	chr8:95556959-95556960	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs75537904	chr8:95556986-95556987	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs568686334	chr8:95556988-95556989	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs537679106	chr8:95556995-95556996	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs547113567	chr8:95556996-95556997	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs557946651	chr8:95557029-95557030	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs571621282	chr8:95557108-95557109	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs534304331	chr8:95557118-95557119	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs186593527	chr8:95557186-95557187	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs560518939	chr8:95557199-95557200	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs78653369	chr8:95557200-95557201	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs11991172	chr8:95557208-95557209	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs150694846	chr8:95557256-95557257	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs543340969	chr8:95557275-95557276	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs564654373	chr8:95557323-95557324	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs190599193	chr8:95557419-95557420	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545239506	chr8:95557451-95557452	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs565476318	chr8:95557457-95557458	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs112702178	chr8:95557459-95557460	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs59321823	chr8:95557522-95557523	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs569627714	chr8:95557528-95557529	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Acute lymphoblastic leukemia	18458336	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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95497200-95564200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:95532800-95558800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr8:95536600-95557000	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr8:95536800-95556600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:95537000-95557400	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr8:95537000-95558600	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr8:95541600-95563600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:95541600-95563800	Weak transcription	Stomach Mucosa	stomach
9	chr8:95543200-95563200	Weak transcription	Fetal Brain Male	brain
10	chr8:95543200-95564800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr8:95543200-95564800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:95543600-95558000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:95543600-95564000	Weak transcription	HSMMtube	muscle
14	chr8:95544400-95558000	Strong transcription	Primary B cells from peripheral blood	blood
15	chr8:95545200-95564000	Weak transcription	Psoas Muscle	Psoas
16	chr8:95546200-95564800	Weak transcription	Esophagus	oesophagus
17	chr8:95546400-95564000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr8:95546400-95564000	Weak transcription	Aorta	Aorta
19	chr8:95546600-95563600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr8:95546800-95558400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr8:95546800-95563600	Weak transcription	Brain Angular Gyrus	brain
22	chr8:95547000-95563000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:95547000-95564000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr8:95547000-95565000	Weak transcription	Pancreas	Pancrea
25	chr8:95547200-95563200	Weak transcription	Gastric	stomach
26	chr8:95547400-95563200	Weak transcription	Brain Substantia Nigra	brain
27	chr8:95547400-95563600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr8:95548000-95563600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr8:95548400-95563800	Weak transcription	Brain Hippocampus Middle	brain
30	chr8:95548400-95563800	Weak transcription	Small Intestine	intestine
31	chr8:95548800-95564000	Weak transcription	Colonic Mucosa	Colon
32	chr8:95549000-95558800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr8:95549000-95563000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr8:95549000-95563800	Weak transcription	HUVEC	blood vessel
35	chr8:95549000-95564000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr8:95549000-95564000	Weak transcription	Brain Germinal Matrix	brain
37	chr8:95549400-95561800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr8:95549400-95563200	Weak transcription	Ovary	ovary
39	chr8:95549400-95563400	Weak transcription	NHDF-Ad	bronchial
40	chr8:95549400-95564000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr8:95549600-95563800	Weak transcription	Brain Anterior Caudate	brain
42	chr8:95550000-95563600	Weak transcription	NH-A	brain
43	chr8:95550400-95563200	Weak transcription	Fetal Brain Female	brain
44	chr8:95550600-95564000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr8:95550600-95564400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr8:95551600-95564800	Weak transcription	Thymus	Thymus
47	chr8:95552000-95563600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr8:95552200-95561000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:95552200-95561000	Weak transcription	Left Ventricle	heart
50	chr8:95552200-95561200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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