Variant report

Variant	nsv438072
Chromosome Location	chr8:95558694-95571443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:916)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 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	chr8:95561953-95561992	K562	blood:	n/a	n/a
2	ARID3A	chr8:95569910-95569916	K562	blood:	n/a	n/a
3	ARID3A	chr8:95565426-95566634	HepG2	liver:	n/a	n/a
4	ATF1	chr8:95569899-95570225	K562	blood:	n/a	n/a
5	ATF1	chr8:95561825-95562110	K562	blood:	n/a	n/a
6	ATF1	chr8:95565579-95566141	K562	blood:	n/a	n/a
7	ATF2	chr8:95565395-95566440	GM12878	blood:	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	chr8:95565566-95566121	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr8:95565622-95565918	K562	blood:	n/a	n/a
12	ATF3	chr8:95565427-95566185	A549	lung:	n/a	n/a
13	ATF3	chr8:95565322-95566218	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	chr8:95565360-95566282	A549	lung:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
17	BCL3	chr8:95565367-95566295	A549	lung:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
18	BCLAF1	chr8:95565527-95566107	K562	blood:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
19	BCLAF1	chr8:95565466-95566185	GM12878	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	chr8:95565323-95566674	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:95565477-95566450	HepG2	liver:	n/a	n/a
23	BHLHE40	chr8:95565474-95566799	K562	blood:	n/a	n/a
24	BRCA1	chr8:95564895-95565001	HepG2	liver:	n/a	n/a
25	BRCA1	chr8:95565594-95566030	HepG2	liver:	n/a	n/a
26	BRCA1	chr8:95565670-95566434	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr8:95565462-95566279	Hela-S3	cervix:	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	chr8:95565523-95566485	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:95565531-95566094	K562	blood:	n/a	n/a
34	CEBPB	chr8:95565353-95566299	GM12878	blood:	n/a	n/a
35	CEBPB	chr8:95565701-95566473	K562	blood:	n/a	n/a
36	CEBPB	chr8:95565550-95566466	A549	lung:	n/a	n/a
37	CEBPB	chr8:95565764-95566115	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:95565519-95566425	A549	lung:	n/a	n/a
39	CEBPB	chr8:95565702-95566387	HepG2	liver:	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	chr8:95565488-95566133	K562	blood:	n/a	n/a
43	CEBPD	chr8:95565448-95566126	HepG2	liver:	n/a	n/a
44	CHD1	chr8:95566013-95566310	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr8:95566496-95566694	GM12878	blood:	n/a	n/a
46	CHD1	chr8:95565345-95566250	GM12878	blood:	n/a	n/a
47	CHD2	chr8:95565549-95566324	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr8:95565396-95566420	GM12878	blood:	n/a	n/a
49	CHD2	chr8:95565311-95566352	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr8:95565608-95566178	K562	blood:	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	chr8:95564335-95564385	Caco-2	colon:	n/a
2	chr8:95564335-95564385	Caco-2	colon:	n/a
3	chr8:95566380-95566430	HIPEpiC	eye:	n/a
4	chr8:95565249-95565299	Caco-2	colon:	n/a
5	chr8:95566476-95566526	A549	lung:	n/a
6	chr8:95565502-95565552	HEEpiC	esophagus:	n/a
7	chr8:95565682-95565732	HEEpiC	esophagus:	n/a
8	chr8:95569815-95569865	Hepatocyte	liver:	n/a
9	chr8:95566223-95566273	PrEC	prostate:	n/a
10	chr8:95566223-95566273	A549	lung:	n/a
11	chr8:95565801-95565851	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:95563352-95563402	H1-hESC	embryonic stem cell:	embryo
13	chr8:95565953-95566003	A549	lung:	n/a
14	chr8:95563352-95563402	NH-A	brain:	n/a
15	chr8:95565682-95565732	PFSK-1	brain:	n/a
16	chr8:95566223-95566273	H1-hESC	embryonic stem cell:	embryo
17	chr8:95566223-95566273	BJ	skin:	n/a
18	chr8:95565789-95565839	GM12892	blood:	n/a
19	chr8:95566380-95566430	CMK	blood:	n/a
20	chr8:95566476-95566526	HNPCEpiC	eye:	n/a
21	chr8:95564335-95564385	HEK293	kidney:	embryo
22	chr8:95565789-95565839	BJ	skin:	n/a
23	chr8:95565249-95565299	ProgFib	skin:	n/a
24	chr8:95565392-95565442	HIPEpiC	eye:	n/a
25	chr8:95565249-95565299	GM12892	blood:	n/a
26	chr8:95565682-95565732	GM12891	blood:	n/a
27	chr8:95565502-95565552	SK-N-SH_RA	brain:	n/a
28	chr8:95569815-95569865	BJ	skin:	n/a
29	chr8:95566670-95566720	HL-60	blood:	n/a
30	chr8:95565392-95565442	ProgFib	skin:	n/a
31	chr8:95565392-95565442	NH-A	brain:	n/a
32	chr8:95565953-95566003	AG04449	skin:	fetal
33	chr8:95566476-95566526	PrEC	prostate:	n/a
34	chr8:95566223-95566273	AG04450	lung:	fetal
35	chr8:95569815-95569865	HAEpiC	amniotic membrane:	n/a
36	chr8:95566476-95566526	NHBE	bronchial:	n/a
37	chr8:95565249-95565299	Jurkat	blood:	n/a
38	chr8:95565801-95565851	ovcar-3	ovarian:	n/a
39	chr8:95569815-95569865	HIPEpiC	eye:	n/a
40	chr8:95566380-95566430	ECC-1	luminal epithelium:	n/a
41	chr8:95565801-95565851	MCF10A-Er-Src	breast:	n/a
42	chr8:95565392-95565442	GM19239	blood:	n/a
43	chr8:95565502-95565552	GM06990	blood:	n/a
44	chr8:95565502-95565552	RPTEC	kidney:	n/a
45	chr8:95565502-95565552	HNPCEpiC	eye:	n/a
46	chr8:95565502-95565552	HCM	heart:	n/a
47	chr8:95566223-95566273	HCF	heart:	n/a
48	chr8:95563352-95563402	PFSK-1	brain:	n/a
49	chr8:95566223-95566273	AoSMC	blood vessel:	n/a
50	chr8:95566223-95566273	HepG2	liver:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95564633..95567300-chr8:95651331..95653603,2	MCF-7	breast:
2	chr8:95564914..95567104-chr8:95570346..95572285,2	K562	blood:
3	chr8:95563755..95566398-chr8:95651251..95655119,6	MCF-7	breast:
4	chr12:39298720..39299544-chr8:95565528..95566062,2	Hela-S3	cervix:
5	chr8:95556183..95559262-chr8:95651441..95653267,3	MCF-7	breast:
6	chr8:95557664..95559966-chr8:95650412..95652511,2	MCF-7	breast:
7	chr8:95555945..95557652-chr8:95557953..95559866,2	MCF-7	breast:
8	chr8:95565366..95567177-chr8:96036825..96038672,2	K562	blood:
9	chr8:95568828..95570983-chr8:95731754..95733719,2	MCF-7	breast:
10	chr8:95553642..95556255-chr8:95557800..95559824,2	K562	blood:
11	chr8:95537067..95539960-chr8:95561344..95563037,2	MCF-7	breast:
12	chr8:95567356..95569576-chr8:95586722..95588643,2	MCF-7	breast:
13	chr8:95554974..95557880-chr8:95564950..95566849,3	MCF-7	breast:
14	chr8:95569874..95571629-chr8:95571639..95574216,2	K562	blood:
15	chr8:95563440..95569104-chr8:95570985..95573855,6	MCF-7	breast:
16	chr8:95564422..95566417-chr8:95730460..95733624,3	K562	blood:
17	chr8:95564312..95566828-chr8:95731001..95732970,2	MCF-7	breast:
18	chr8:95564818..95567463-chr8:95729750..95733556,7	MCF-7	breast:
19	chr8:95548641..95550186-chr8:95556999..95558731,2	K562	blood:
20	chr8:95558228..95561115-chr8:95906355..95909204,2	K562	blood:
21	chr8:95564422..95566417-chr8:95731300..95733624,2	K562	blood:
22	chr8:95565950..95567882-chr8:95569895..95571408,2	MCF-7	breast:
23	chr8:95567263..95568889-chr8:95730604..95733180,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 512 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1992370	chr8:95558694-95558695	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567730369	chr8:95558729-95558730	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs536767258	chr8:95558736-95558737	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs75351432	chr8:95558758-95558759	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs570070654	chr8:95558761-95558762	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs376277368	chr8:95558770-95558771	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs538957500	chr8:95558804-95558805	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs3102872	chr8:95558813-95558814	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572532025	chr8:95558854-95558855	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs182816502	chr8:95558920-95558921	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs575585575	chr8:95558939-95558940	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs573353979	chr8:95558940-95558941	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs542324404	chr8:95558958-95558959	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs562336468	chr8:95558975-95558976	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs576012121	chr8:95558989-95558990	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs544952530	chr8:95558990-95558991	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs373553295	chr8:95559039-95559040	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs533530232	chr8:95559050-95559051	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs3133651	chr8:95559092-95559093	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558176604	chr8:95559102-95559103	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs535153820	chr8:95559128-95559129	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs370693368	chr8:95559129-95559130	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs547292415	chr8:95559139-95559140	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs12334990	chr8:95559186-95559187	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs530206063	chr8:95559225-95559226	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs550294369	chr8:95559228-95559229	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs569926843	chr8:95559262-95559263	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs539054899	chr8:95559293-95559294	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs552304218	chr8:95559308-95559309	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs140437008	chr8:95559310-95559311	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs534988322	chr8:95559328-95559329	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs58408347	chr8:95559348-95559349	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574733478	chr8:95559425-95559426	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs535963674	chr8:95559440-95559441	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs187534886	chr8:95559532-95559533	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs575931943	chr8:95559664-95559665	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs75749689	chr8:95559715-95559716	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs558293781	chr8:95559758-95559759	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs144283476	chr8:95559836-95559837	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs377198160	chr8:95559839-95559840	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs541344626	chr8:95559841-95559842	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs377382849	chr8:95559894-95559895	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs562769566	chr8:95559900-95559901	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs147790211	chr8:95559972-95559973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs148880553	chr8:95559977-95559978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs578118738	chr8:95560009-95560010	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543533276	chr8:95560059-95560060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115292747	chr8:95560072-95560073	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563767546	chr8:95560109-95560110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532520501	chr8:95560141-95560142	Weak transcription Enhancers	Chromatin interactive region	2 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
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr8:95541600-95563600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr8:95541600-95563800	Weak transcription	Stomach Mucosa	stomach
5	chr8:95543200-95563200	Weak transcription	Fetal Brain Male	brain
6	chr8:95543200-95564800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:95543200-95564800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:95543600-95564000	Weak transcription	HSMMtube	muscle
9	chr8:95545200-95564000	Weak transcription	Psoas Muscle	Psoas
10	chr8:95546200-95564800	Weak transcription	Esophagus	oesophagus
11	chr8:95546400-95564000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:95546400-95564000	Weak transcription	Aorta	Aorta
13	chr8:95546600-95563600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:95546800-95563600	Weak transcription	Brain Angular Gyrus	brain
15	chr8:95547000-95563000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:95547000-95564000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr8:95547000-95565000	Weak transcription	Pancreas	Pancrea
18	chr8:95547200-95563200	Weak transcription	Gastric	stomach
19	chr8:95547400-95563200	Weak transcription	Brain Substantia Nigra	brain
20	chr8:95547400-95563600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr8:95548000-95563600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:95548400-95563800	Weak transcription	Brain Hippocampus Middle	brain
23	chr8:95548400-95563800	Weak transcription	Small Intestine	intestine
24	chr8:95548800-95564000	Weak transcription	Colonic Mucosa	Colon
25	chr8:95549000-95558800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr8:95549000-95563000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:95549000-95563800	Weak transcription	HUVEC	blood vessel
28	chr8:95549000-95564000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr8:95549000-95564000	Weak transcription	Brain Germinal Matrix	brain
30	chr8:95549400-95561800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr8:95549400-95563200	Weak transcription	Ovary	ovary
32	chr8:95549400-95563400	Weak transcription	NHDF-Ad	bronchial
33	chr8:95549400-95564000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr8:95549600-95563800	Weak transcription	Brain Anterior Caudate	brain
35	chr8:95550000-95563600	Weak transcription	NH-A	brain
36	chr8:95550400-95563200	Weak transcription	Fetal Brain Female	brain
37	chr8:95550600-95564000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr8:95550600-95564400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr8:95551600-95564800	Weak transcription	Thymus	Thymus
40	chr8:95552000-95563600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr8:95552200-95561000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr8:95552200-95561000	Weak transcription	Left Ventricle	heart
43	chr8:95552200-95561200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr8:95552200-95562000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr8:95552200-95563000	Weak transcription	Right Ventricle	heart
46	chr8:95552200-95563600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:95552200-95563600	Weak transcription	NHLF	lung
48	chr8:95552200-95563800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:95552200-95565000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr8:95552400-95559200	Weak transcription	Primary B cells from cord blood	blood

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