Variant report

Variant	nsv889739
Chromosome Location	chr8:1898547-1918352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:2135)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 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	ATF1	chr8:1905426-1905729	K562	blood:	n/a	n/a
2	BACH1	chr8:1908240-1908440	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:1900444-1900619	K562	blood:	n/a	chr8:1900518-1900531
4	BHLHE40	chr8:1911161-1911462	K562	blood:	n/a	n/a
5	BHLHE40	chr8:1906190-1906595	K562	blood:	n/a	n/a
6	BHLHE40	chr8:1898324-1898578	K562	blood:	n/a	n/a
7	BHLHE40	chr8:1904080-1904391	K562	blood:	n/a	n/a
8	BHLHE40	chr8:1904989-1905720	K562	blood:	n/a	n/a
9	CEBPB	chr8:1908125-1908384	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:1905506-1905747	K562	blood:	n/a	n/a
11	CEBPB	chr8:1908196-1908486	MCF-7	breast:	n/a	n/a
12	CEBPB	chr8:1905512-1905727	K562	blood:	n/a	n/a
13	CEBPB	chr8:1908278-1908309	K562	blood:	n/a	n/a
14	CEBPB	chr8:1917870-1918070	K562	blood:	n/a	n/a
15	CEBPB	chr8:1917852-1918103	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:1914793-1914975	K562	blood:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
17	CEBPB	chr8:1914751-1915120	IMR90	lung:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
18	CEBPB	chr8:1907993-1908601	HCT-116	colon:	n/a	n/a
19	CEBPB	chr8:1905439-1905837	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:1908171-1908466	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:1901757-1901948	K562	blood:	n/a	chr8:1901763-1901774
22	CEBPB	chr8:1908101-1908510	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:1917911-1918068	A549	lung:	n/a	n/a
24	CEBPB	chr8:1901636-1901913	HepG2	liver:	n/a	chr8:1901763-1901774
25	CREB1	chr8:1916103-1916317	A549	lung:	n/a	chr8:1916249-1916262
26	CREB1	chr8:1916164-1916330	A549	lung:	n/a	chr8:1916249-1916262
27	CTCF	chr8:1905160-1905310	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr8:1905000-1905150	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr8:1905640-1905790	AG10803	skin:	n/a	n/a
30	CTCF	chr8:1908380-1908530	SAEC	small airway:	n/a	n/a
31	CTCF	chr8:1908604-1908632	Lung_OC	lung:	n/a	n/a
32	CTCF	chr8:1903601-1903727	GM20000	blood:	n/a	n/a
33	CUX1	chr8:1904807-1905255	K562	blood:	n/a	n/a
34	ELF1	chr8:1903653-1903893	GM12878	blood:	n/a	n/a
35	EP300	chr8:1903023-1903935	GM12878	blood:	n/a	n/a
36	EP300	chr8:1908328-1908355	K562	blood:	n/a	n/a
37	EP300	chr8:1899415-1899494	K562	blood:	n/a	n/a
38	EP300	chr8:1903499-1903901	GM12878	blood:	n/a	n/a
39	EP300	chr8:1905475-1905770	K562	blood:	n/a	n/a
40	FOS	chr8:1908198-1908414	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:1908169-1908531	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:1908156-1908649	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr8:1908198-1908727	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL1	chr8:1904946-1905248	K562	blood:	n/a	n/a
45	FOXA1	chr8:1911369-1911679	T-47D	breast:	n/a	chr8:1911533-1911545
46	FOXA2	chr8:1916162-1916884	A549	lung:	n/a	n/a
47	FOXA2	chr8:1916248-1916806	A549	lung:	n/a	n/a
48	FOXM1	chr8:1903037-1903986	GM12878	blood:	n/a	n/a
49	FOXP2	chr8:1916353-1916623	PFSK-1	brain:	n/a	n/a
50	FOXP2	chr8:1904902-1905510	PFSK-1	brain:	n/a	n/a

(count:2135 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1900400-1900450	Jurkat	blood:	n/a
2	chr8:1908301-1908351	T-47D	breast:	n/a
3	chr8:1914991-1915041	AoSMC	blood vessel:	n/a
4	chr8:1906338-1906388	AoSMC	blood vessel:	n/a
5	chr8:1900992-1901042	PFSK-1	brain:	n/a
6	chr8:1899127-1899177	BJ	skin:	n/a
7	chr8:1915004-1915054	PANC-1	pancreas:	n/a
8	chr8:1908301-1908351	NB4	blood:	n/a
9	chr8:1913132-1913182	BE2_C	brain:	n/a
10	chr8:1900778-1900828	LNCaP	prostate:	n/a
11	chr8:1913132-1913182	HCM	heart:	n/a
12	chr8:1900089-1900139	SK-N-SH	brain:	n/a
13	chr8:1914991-1915041	GM19239	blood:	n/a
14	chr8:1900778-1900828	HRE	kidney:	n/a
15	chr8:1905343-1905393	AG04449	skin:	fetal
16	chr8:1905131-1905181	MCF10A-Er-Src	breast:	n/a
17	chr8:1899231-1899281	RPTEC	kidney:	n/a
18	chr8:1915076-1915126	HUVEC	blood vessel:	n/a
19	chr8:1913086-1913136	NT2-D1	testis:	n/a
20	chr8:1905131-1905181	PFSK-1	brain:	n/a
21	chr8:1900892-1900942	IMR90	lung:	fetal
22	chr8:1899231-1899281	HRE	kidney:	n/a
23	chr8:1915004-1915054	SK-N-SH_RA	brain:	n/a
24	chr8:1899538-1899588	IMR90	lung:	fetal
25	chr8:1900353-1900403	SK-N-SH_RA	brain:	n/a
26	chr8:1914991-1915041	HCF	heart:	n/a
27	chr8:1906498-1906548	PANC-1	pancreas:	n/a
28	chr8:1900353-1900403	BE2_C	brain:	n/a
29	chr8:1899231-1899281	ECC-1	luminal epithelium:	n/a
30	chr8:1914991-1915041	T-47D	breast:	n/a
31	chr8:1913269-1913319	HAEpiC	amniotic membrane:	n/a
32	chr8:1906418-1906468	A549	lung:	n/a
33	chr8:1914991-1915041	HepG2	liver:	n/a
34	chr8:1900191-1900241	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:1911588-1911638	IMR90	lung:	fetal
36	chr8:1916285-1916335	HRE	kidney:	n/a
37	chr8:1916285-1916335	HRPEpiC	eye:	n/a
38	chr8:1899468-1899518	HNPCEpiC	eye:	n/a
39	chr8:1899468-1899518	AG04449	skin:	fetal
40	chr8:1900992-1901042	HNPCEpiC	eye:	n/a
41	chr8:1900992-1901042	HAEpiC	amniotic membrane:	n/a
42	chr8:1908301-1908351	HAEpiC	amniotic membrane:	n/a
43	chr8:1914991-1915041	GM06990	blood:	n/a
44	chr8:1913086-1913136	H1-hESC	embryonic stem cell:	embryo
45	chr8:1908301-1908351	AG10803	skin:	n/a
46	chr8:1899231-1899281	GM12891	blood:	n/a
47	chr8:1899127-1899177	SK-N-SH	brain:	n/a
48	chr8:1899538-1899588	GM12878	blood:	n/a
49	chr8:1906312-1906362	HMEC	breast:	n/a
50	chr8:1913132-1913182	GM12892	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
2	chr8:1907491..1909196-chr8:1911477..1913920,2	K562	blood:
3	chr8:1907491..1909196-chr8:1911477..1913920,2	K562	blood:
4	chr8:1887349..1889723-chr8:1904508..1906219,2	K562	blood:
5	chr8:1900404..1902135-chr8:1904270..1906707,2	K562	blood:
6	chr8:1869392..1872141-chr8:1901807..1903545,2	K562	blood:
7	chr8:1904438..1906943-chr8:1908364..1910920,2	K562	blood:
8	chr8:1911383..1914358-chr8:1918883..1921800,2	MCF-7	breast:
9	chr8:1876158..1879042-chr8:1903928..1907345,3	K562	blood:
10	chr8:1902551..1904412-chr8:1906073..1908055,2	K562	blood:
11	chr8:1905928..1907788-chr8:1909949..1911807,2	MCF-7	breast:
12	chr8:1904438..1906943-chr8:1908364..1910920,2	K562	blood:
13	chr8:1905928..1907788-chr8:1909949..1911807,2	MCF-7	breast:
14	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
15	chr8:1902551..1904412-chr8:1906073..1908055,2	K562	blood:
16	chr8:1900404..1902135-chr8:1904270..1906707,2	K562	blood:
17	chr8:1910618..1913298-chr8:1921170..1922936,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-18	chr8:1908721-1909149	l_3533_chr8:1906703-1909044_brain
2	lnc-CSMD1-18	chr8:1906704-1908609	l_3533_chr8:1906703-1909044_brain

No data

Variant related genes	Relation type
ENSG00000270988	TF binding region
KBTBD11-OT1	TF binding region
KBTBD11	TF binding region
ENSG00000270988	CpG island
KBTBD11-OT1	CpG island
KBTBD11	CpG island
ENSG00000253764	chromatin interactions
ENSG00000176595	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000253696	chromatin interactions

Extended variants
information (count: 1252 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17064417	chr8:1898547-1898548	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572475926	chr8:1898557-1898558	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149044814	chr8:1898614-1898615	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144870741	chr8:1898652-1898653	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138778821	chr8:1898655-1898656	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183958669	chr8:1898681-1898682	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566404844	chr8:1898685-1898686	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189418460	chr8:1898785-1898786	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551775114	chr8:1898803-1898804	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555107312	chr8:1898817-1898818	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181309778	chr8:1898854-1898855	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141723362	chr8:1898855-1898856	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368467436	chr8:1898871-1898872	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570907990	chr8:1898897-1898898	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77380111	chr8:1898913-1898914	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71211528	chr8:1898916-1898917	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142740034	chr8:1898918-1898919	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111858629	chr8:1898930-1898931	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567537073	chr8:1898938-1898939	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13268639	chr8:1898965-1898966	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563959897	chr8:1898966-1898967	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569272266	chr8:1899009-1899010	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538668268	chr8:1899038-1899039	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374096172	chr8:1899086-1899087	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532887361	chr8:1899132-1899133	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558571193	chr8:1899145-1899146	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572334627	chr8:1899151-1899152	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73671066	chr8:1899170-1899171	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs554776075	chr8:1899183-1899184	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574687230	chr8:1899196-1899197	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368095419	chr8:1899231-1899232	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs543103066	chr8:1899249-1899250	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs563010747	chr8:1899288-1899289	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs576352417	chr8:1899289-1899290	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs545411237	chr8:1899301-1899302	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs565422749	chr8:1899372-1899373	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs373288297	chr8:1899374-1899375	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs544996790	chr8:1899378-1899379	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs111991668	chr8:1899382-1899383	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs190076240	chr8:1899395-1899396	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs561102234	chr8:1899404-1899405	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs141447303	chr8:1899412-1899413	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs181423005	chr8:1899415-1899416	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549458913	chr8:1899425-1899426	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs569459034	chr8:1899438-1899439	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs58854534	chr8:1899446-1899447	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs371982936	chr8:1899449-1899450	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs530243462	chr8:1899480-1899481	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs567407604	chr8:1899490-1899491	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs570572359	chr8:1899495-1899496	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1845400-1908000	Weak transcription	Right Atrium	heart
2	chr8:1868000-1902400	Strong transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:1871600-1907400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:1880800-1906200	Weak transcription	Colonic Mucosa	Colon
5	chr8:1884400-1904800	Weak transcription	Brain Germinal Matrix	brain
6	chr8:1884600-1906200	Weak transcription	A549	lung
7	chr8:1885400-1900000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:1886000-1906200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:1887800-1900400	Weak transcription	Gastric	stomach
10	chr8:1888000-1904800	Weak transcription	HMEC	breast
11	chr8:1889400-1905000	Weak transcription	HSMM	muscle
12	chr8:1889400-1910000	Weak transcription	HUVEC	blood vessel
13	chr8:1890000-1911000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:1891200-1906000	Weak transcription	Fetal Heart	heart
15	chr8:1891600-1907400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:1891800-1906200	Weak transcription	Colon Smooth Muscle	Colon
17	chr8:1892000-1899600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:1892000-1901200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:1892200-1906000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr8:1892400-1899400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:1892400-1900000	Strong transcription	H9 Cell Line	embryonic stem cell
22	chr8:1892400-1901000	Genic enhancers	Fetal Muscle Leg	muscle
23	chr8:1892800-1900000	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr8:1893000-1898600	Strong transcription	H1 Cell Line	embryonic stem cell
25	chr8:1893200-1898800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
26	chr8:1893400-1898600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:1894000-1900200	Weak transcription	Pancreas	Pancrea
28	chr8:1894000-1903800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:1894000-1904800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr8:1894200-1904800	Weak transcription	Ovary	ovary
31	chr8:1894200-1905000	Weak transcription	Fetal Intestine Small	intestine
32	chr8:1894400-1900400	Enhancers	Thymus	Thymus
33	chr8:1894600-1900600	Weak transcription	Right Ventricle	heart
34	chr8:1894800-1900200	Weak transcription	Aorta	Aorta
35	chr8:1894800-1900400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:1895200-1904600	Weak transcription	Fetal Lung	lung
37	chr8:1895400-1899800	Weak transcription	Brain Substantia Nigra	brain
38	chr8:1895400-1901600	Weak transcription	NHDF-Ad	bronchial
39	chr8:1895600-1900000	Weak transcription	Brain Anterior Caudate	brain
40	chr8:1895600-1900400	Weak transcription	Brain Angular Gyrus	brain
41	chr8:1895600-1901000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:1895600-1901000	Genic enhancers	Fetal Muscle Trunk	muscle
43	chr8:1895600-1902000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr8:1895600-1904800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:1895600-1905600	Weak transcription	NHLF	lung
46	chr8:1895600-1906200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr8:1895600-1907000	Weak transcription	Fetal Intestine Large	intestine
48	chr8:1895800-1901600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:1896000-1898600	Enhancers	Primary hematopoietic stem cells	blood
50	chr8:1896000-1898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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