Variant report

Variant	nsv1034343
Chromosome Location	chr8:9948342-10014155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10009672-10010165	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:10009586-10009863	K562	blood:	n/a	n/a
3	BACH1	chr8:9953856-9953925	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:9988646-9988815	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:10009852-10010062	H1-hESC	embryonic stem cell:	n/a	chr8:10009959-10009973
6	BCL3	chr8:10009722-10010009	GM12878	blood:	n/a	n/a
7	BCL3	chr8:10002131-10002433	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:9951335-9951662	K562	blood:	n/a	n/a
9	BHLHE40	chr8:9951427-9951617	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:9966233-9966301	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:9951338-9951626	HepG2	liver:	n/a	n/a
12	BHLHE40	chr8:9951404-9951632	A549	lung:	n/a	n/a
13	BHLHE40	chr8:9956535-9956793	K562	blood:	n/a	chr8:9956727-9956736 chr8:9956721-9956742 chr8:9956727-9956736 chr8:9956726-9956735 chr8:9956725-9956738
14	BRCA1	chr8:10009571-10010154	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr8:9951269-9951622	K562	blood:	n/a	n/a
16	CBX3	chr8:10009275-10010611	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:9951264-9951752	HCT-116	colon:	n/a	n/a
18	CBX3	chr8:9951256-9951610	K562	blood:	n/a	n/a
19	CBX3	chr8:9951179-9951780	HCT-116	colon:	n/a	n/a
20	CEBPB	chr8:9996071-9996429	IMR90	lung:	n/a	chr8:9996234-9996245 chr8:9996236-9996247
21	CEBPB	chr8:9996107-9996375	HepG2	liver:	n/a	chr8:9996234-9996245 chr8:9996236-9996247
22	CEBPB	chr8:9983082-9983451	HepG2	liver:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
23	CEBPB	chr8:9998053-9998131	A549	lung:	n/a	n/a
24	CEBPB	chr8:9963119-9963474	IMR90	lung:	n/a	chr8:9963296-9963305 chr8:9963294-9963305 chr8:9963294-9963307 chr8:9963295-9963306 chr8:9963379-9963390
25	CEBPB	chr8:10009791-10010095	A549	lung:	n/a	n/a
26	CEBPB	chr8:9967365-9967573	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:10009765-10010031	A549	lung:	n/a	n/a
28	CEBPB	chr8:9983078-9983453	IMR90	lung:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
29	CEBPB	chr8:9983084-9983448	A549	lung:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
30	CEBPB	chr8:9956037-9956273	K562	blood:	n/a	chr8:9956142-9956153 chr8:9956140-9956153
31	CEBPB	chr8:10009447-10010478	HCT-116	colon:	n/a	n/a
32	CEBPB	chr8:10009548-10010105	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:9983081-9983450	K562	blood:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
34	CEBPB	chr8:9983236-9983318	H1-hESC	embryonic stem cell:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
35	CEBPB	chr8:9983109-9983432	Hela-S3	cervix:	n/a	chr8:9983262-9983271 chr8:9983262-9983271 chr8:9983260-9983271 chr8:9983262-9983271 chr8:9983260-9983273 chr8:9983262-9983271
36	CEBPB	chr8:10009561-10010170	A549	lung:	n/a	n/a
37	CEBPB	chr8:9996074-9996419	Hela-S3	cervix:	n/a	chr8:9996234-9996245 chr8:9996236-9996247
38	CEBPB	chr8:10002239-10002387	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:9963157-9963448	K562	blood:	n/a	chr8:9963296-9963305 chr8:9963294-9963305 chr8:9963294-9963307 chr8:9963295-9963306 chr8:9963379-9963390
40	CEBPB	chr8:10009294-10010182	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr8:9963103-9963475	H1-hESC	embryonic stem cell:	n/a	chr8:9963296-9963305 chr8:9963294-9963305 chr8:9963294-9963307 chr8:9963295-9963306 chr8:9963379-9963390
42	CEBPB	chr8:9963136-9963459	A549	lung:	n/a	chr8:9963296-9963305 chr8:9963294-9963305 chr8:9963294-9963307 chr8:9963295-9963306 chr8:9963379-9963390
43	CEBPB	chr8:10009997-10010154	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:9963121-9963458	HepG2	liver:	n/a	chr8:9963296-9963305 chr8:9963294-9963305 chr8:9963294-9963307 chr8:9963295-9963306 chr8:9963379-9963390
45	CHD2	chr8:10009778-10010102	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr8:10008540-10008690	NHEK	skin:	n/a	n/a
47	CTCF	chr8:9981426-9981535	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:9974242-9974295	GM10248	blood:	n/a	n/a
49	CTCF	chr8:10008633-10008641	NHEK	skin:	n/a	n/a
50	CTCF	chr8:9997260-9997410	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10005590-10005640	ECC-1	luminal epithelium:	n/a
2	chr8:10005474-10005524	K562	blood:	n/a
3	chr8:9986782-9986832	HNPCEpiC	eye:	n/a
4	chr8:9952965-9953015	Caco-2	colon:	n/a
5	chr8:10005474-10005524	PrEC	prostate:	n/a
6	chr8:10005590-10005640	ECC-1	luminal epithelium:	n/a
7	chr8:10005474-10005524	K562	blood:	n/a
8	chr8:9986782-9986832	HNPCEpiC	eye:	n/a
9	chr8:9952965-9953015	Caco-2	colon:	n/a
10	chr8:10005474-10005524	PrEC	prostate:	n/a
11	chr8:10005474-10005524	PFSK-1	brain:	n/a
12	chr8:10001523-10001573	BJ	skin:	n/a
13	chr8:10001523-10001573	HMEC	breast:	n/a
14	chr8:9987847-9987897	HepG2	liver:	n/a
15	chr8:9996632-9996682	BE2_C	brain:	n/a
16	chr8:10001627-10001677	PANC-1	pancreas:	n/a
17	chr8:10001523-10001573	AG09319	gingival:	n/a
18	chr8:10001612-10001662	HL-60	blood:	n/a
19	chr8:9952636-9952686	NH-A	brain:	n/a
20	chr8:10005474-10005524	HRCEpiC	kidney:	n/a
21	chr8:10005590-10005640	GM12878	blood:	n/a
22	chr8:9952636-9952686	HRPEpiC	eye:	n/a
23	chr8:9965554-9965604	GM12892	blood:	n/a
24	chr8:9986782-9986832	HUVEC	blood vessel:	n/a
25	chr8:9986782-9986832	NB4	blood:	n/a
26	chr8:10005590-10005640	AG04449	skin:	fetal
27	chr8:9952926-9952976	PANC-1	pancreas:	n/a
28	chr8:10005590-10005640	HCPEpiC	choroid plexus:	n/a
29	chr8:10001612-10001662	GM19239	blood:	n/a
30	chr8:9951983-9952033	HEK293	kidney:	embryo
31	chr8:9953022-9953072	HUVEC	blood vessel:	n/a
32	chr8:10001523-10001573	HEK293	kidney:	embryo
33	chr8:9986782-9986832	ProgFib	skin:	n/a
34	chr8:9996632-9996682	HRCEpiC	kidney:	n/a
35	chr8:10001612-10001662	SK-N-SH_RA	brain:	n/a
36	chr8:9957329-9957379	NB4	blood:	n/a
37	chr8:9953022-9953072	IMR90	lung:	fetal
38	chr8:9996632-9996682	H1-hESC	embryonic stem cell:	embryo
39	chr8:9957329-9957379	BJ	skin:	n/a
40	chr8:10001523-10001573	Jurkat	blood:	n/a
41	chr8:9952965-9953015	HNPCEpiC	eye:	n/a
42	chr8:9951983-9952033	HIPEpiC	eye:	n/a
43	chr8:9957329-9957379	MCF-7	breast:	n/a
44	chr8:9965554-9965604	HCT-116	colon:	n/a
45	chr8:9987847-9987897	HNPCEpiC	eye:	n/a
46	chr8:9986782-9986832	HRPEpiC	eye:	n/a
47	chr8:10005423-10005473	SKMC	muscle:	n/a
48	chr8:9952926-9952976	NHBE	bronchial:	n/a
49	chr8:9965554-9965604	Caco-2	colon:	n/a
50	chr8:9996632-9996682	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:9959952..9962225-chr8:9964575..9967404,2	MCF-7	breast:
2	chr8:9968733..9972257-chr8:9973876..9975676,3	K562	blood:
3	chr8:9951257..9953099-chr8:9953951..9956586,3	MCF-7	breast:
4	chr8:9989052..9991739-chr8:9991879..9993683,2	K562	blood:
5	chr8:9963502..9966052-chr8:9972558..9974638,2	MCF-7	breast:
6	chr8:9968733..9972257-chr8:9973876..9975676,3	K562	blood:
7	chr8:9963502..9966052-chr8:9972558..9974638,2	MCF-7	breast:
8	chr8:9989052..9991739-chr8:9991879..9993683,2	K562	blood:
9	chr8:9954771..9956774-chr8:9960148..9962685,2	K562	blood:
10	chr8:9911729..9913700-chr8:9963859..9966058,2	MCF-7	breast:
11	chr8:9910777..9912807-chr8:10008037..10009823,2	MCF-7	breast:
12	chr8:9954771..9956774-chr8:9960148..9962685,2	K562	blood:
13	chr19:10063347..10063968-chr8:9970215..9971121,2	MCF-7	breast:
14	chr8:9985940..9988660-chr8:9990986..9993361,2	K562	blood:
15	chr8:9985940..9988660-chr8:9990986..9993361,2	K562	blood:
16	chr8:9985280..9987758-chr8:9989379..9992085,2	K562	blood:
17	chr8:9985280..9987758-chr8:9989379..9992085,2	K562	blood:
18	chr8:9959952..9962225-chr8:9964575..9967404,2	MCF-7	breast:

Variant related genes	Relation type
MSRA	TF binding region
MSRA	CpG island
ENSG00000175806	chromatin interactions
ENSG00000260093	chromatin interactions

Extended variants
information (count: 3793 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:3793 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544512320	chr8:9948403-9948404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577509587	chr8:9948430-9948431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6988046	chr8:9948433-9948434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs530061876	chr8:9948438-9948439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547035867	chr8:9948495-9948496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373255317	chr8:9948502-9948503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560411408	chr8:9948507-9948508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375162631	chr8:9948527-9948528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112098178	chr8:9948548-9948549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369456307	chr8:9948565-9948566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538092372	chr8:9948571-9948572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548528316	chr8:9948581-9948582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75107534	chr8:9948599-9948600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533584980	chr8:9948607-9948608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369957996	chr8:9948610-9948611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553806728	chr8:9948616-9948617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79840240	chr8:9948634-9948635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373953069	chr8:9948661-9948662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562202950	chr8:9948662-9948663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545484459	chr8:9948676-9948677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7012221	chr8:9948701-9948702	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558684076	chr8:9948728-9948729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183205042	chr8:9948738-9948739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144449557	chr8:9948765-9948766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200172273	chr8:9948782-9948783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561262212	chr8:9948787-9948788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188085889	chr8:9948790-9948791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10087802	chr8:9948874-9948875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560626901	chr8:9948905-9948906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192706310	chr8:9948909-9948910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184502925	chr8:9948943-9948944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373160303	chr8:9948950-9948951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570984772	chr8:9948995-9948996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186681859	chr8:9948999-9949000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541415151	chr8:9949005-9949006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372779526	chr8:9949016-9949017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192298676	chr8:9949022-9949023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184769275	chr8:9949032-9949033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7012397	chr8:9949033-9949034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs9644718	chr8:9949048-9949049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs112047939	chr8:9949057-9949058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539098790	chr8:9949061-9949062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181867859	chr8:9949073-9949074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569075416	chr8:9949111-9949112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377691325	chr8:9949117-9949118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199796988	chr8:9949119-9949120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113904163	chr8:9949120-9949121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140394227	chr8:9949171-9949172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112342391	chr8:9949173-9949174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184809645	chr8:9949179-9949180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9940000-9949400	Weak transcription	Spleen	Spleen
2	chr8:9940200-9948600	Weak transcription	Primary T cells from cord blood	blood
3	chr8:9945200-9950000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr8:9947000-9948400	Enhancers	HMEC	breast
5	chr8:9947200-9948600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:9947800-9948600	Enhancers	Osteobl	bone
7	chr8:9947800-9949800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:9948000-9951400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:9948200-9948600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:9948200-9952800	Weak transcription	NHDF-Ad	bronchial
11	chr8:9949800-9950800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:9951000-9951800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
13	chr8:9951200-9951800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
14	chr8:9951400-9952000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:9952000-9959400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:9952400-9952800	Enhancers	Fetal Brain Male	brain
17	chr8:9952600-9952800	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:9952600-9952800	Enhancers	Brain Germinal Matrix	brain
19	chr8:9952600-9953000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:9952600-9955200	Active TSS	Brain Anterior Caudate	brain
21	chr8:9952600-9955200	Active TSS	Brain Hippocampus Middle	brain
22	chr8:9952600-9956800	Active TSS	Fetal Brain Female	brain
23	chr8:9952800-9953200	Flanking Active TSS	Brain Germinal Matrix	brain
24	chr8:9952800-9953200	Flanking Active TSS	Fetal Brain Male	brain
25	chr8:9952800-9955000	Active TSS	Brain Cingulate Gyrus	brain
26	chr8:9952800-9955000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:9952800-9955400	Active TSS	Brain Angular Gyrus	brain
28	chr8:9952800-9955400	Active TSS	NH-A	brain
29	chr8:9952800-9955800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:9953000-9953200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr8:9953000-9953400	Enhancers	Right Atrium	heart
32	chr8:9953000-9953800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:9953000-9955000	Active TSS	Brain Substantia Nigra	brain
34	chr8:9953000-9955200	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr8:9953200-9953600	Active TSS	Fetal Brain Male	brain
36	chr8:9953200-9955200	Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr8:9953200-9955800	Active TSS	Brain Germinal Matrix	brain
38	chr8:9953600-9954000	Flanking Active TSS	Fetal Brain Male	brain
39	chr8:9953800-9954000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:9954000-9956200	Active TSS	Fetal Brain Male	brain
41	chr8:9955000-9956600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr8:9955000-9956800	Weak transcription	Brain Substantia Nigra	brain
43	chr8:9955000-9957400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr8:9955200-9955400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr8:9955200-9956400	Weak transcription	Brain Anterior Caudate	brain
46	chr8:9955200-9956400	Weak transcription	Brain Hippocampus Middle	brain
47	chr8:9955200-9957000	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr8:9955400-9956600	Weak transcription	Brain Angular Gyrus	brain
49	chr8:9955800-9956000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:9955800-9956400	Flanking Active TSS	Brain Germinal Matrix	brain

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