Variant report

Variant	nsv1026137
Chromosome Location	chr8:67376420-67408122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:550)
Chromatin interactive
region (count:21)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:67385678-67385869	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:67376527-67376760	HepG2	liver:	n/a	n/a
3	ATF2	chr8:67397821-67398395	GM12878	blood:	n/a	n/a
4	ATF2	chr8:67397862-67398274	GM12878	blood:	n/a	n/a
5	ATF2	chr8:67400567-67400993	GM12878	blood:	n/a	n/a
6	ATF2	chr8:67400544-67401075	GM12878	blood:	n/a	n/a
7	BACH1	chr8:67406671-67406869	H1-hESC	embryonic stem cell:	n/a	chr8:67406699-67406713
8	BHLHE40	chr8:67404458-67404495	K562	blood:	n/a	n/a
9	BHLHE40	chr8:67397932-67398528	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:67405978-67406157	K562	blood:	n/a	chr8:67406016-67406025 chr8:67406014-67406027 chr8:67406015-67406024 chr8:67406010-67406031 chr8:67406016-67406025
11	BHLHE40	chr8:67400587-67401234	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:67406379-67406986	K562	blood:	n/a	n/a
13	BRCA1	chr8:67383595-67383967	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr8:67389916-67390143	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr8:67383537-67383999	HCT-116	colon:	n/a	n/a
16	CBX3	chr8:67385302-67385959	HCT-116	colon:	n/a	n/a
17	CEBPB	chr8:67398113-67398309	HepG2	liver:	n/a	chr8:67398151-67398162
18	CEBPB	chr8:67395823-67396125	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:67385016-67385148	H1-hESC	embryonic stem cell:	n/a	chr8:67385137-67385148
20	CEBPB	chr8:67403961-67404105	A549	lung:	n/a	chr8:67404012-67404023
21	CEBPB	chr8:67383582-67383903	A549	lung:	n/a	n/a
22	CEBPB	chr8:67383544-67383955	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:67384997-67385194	A549	lung:	n/a	chr8:67385137-67385148
24	CEBPB	chr8:67385511-67385788	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:67407925-67408204	IMR90	lung:	n/a	chr8:67408064-67408075
26	CEBPB	chr8:67386137-67386462	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:67385092-67385175	HepG2	liver:	n/a	chr8:67385137-67385148
28	CEBPB	chr8:67407995-67408216	HepG2	liver:	n/a	chr8:67408064-67408075
29	CEBPB	chr8:67383447-67384093	A549	lung:	n/a	n/a
30	CEBPB	chr8:67403938-67404180	HepG2	liver:	n/a	chr8:67404012-67404023
31	CEBPB	chr8:67393601-67393691	A549	lung:	n/a	n/a
32	CEBPB	chr8:67384973-67385233	K562	blood:	n/a	chr8:67385137-67385148
33	CEBPB	chr8:67393590-67393751	Hela-S3	cervix:	n/a	chr8:67393690-67393701 chr8:67393690-67393703
34	CEBPB	chr8:67376696-67377167	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:67383127-67383379	A549	lung:	n/a	n/a
36	CEBPB	chr8:67389943-67390258	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:67376884-67377099	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:67383574-67383955	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:67389979-67390289	IMR90	lung:	n/a	n/a
40	CHD2	chr8:67384509-67384728	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:67379241-67379351	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr8:67388920-67389070	GM12875	blood:	n/a	n/a
43	CTCF	chr8:67379280-67379430	GM12864	blood:	n/a	n/a
44	CTCF	chr8:67379242-67379408	A549	lung:	n/a	n/a
45	CTCF	chr8:67388860-67389010	GM12864	blood:	n/a	n/a
46	CTCF	chr8:67379280-67379430	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr8:67379240-67379390	NB4	blood:	n/a	n/a
48	CTCF	chr8:67379276-67379359	GM19240	blood:	n/a	n/a
49	CTCF	chr8:67388940-67389090	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr8:67379238-67379359	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67405257-67405307	SKMC	muscle:	n/a
2	chr8:67405257-67405307	SKMC	muscle:	n/a
3	chr8:67404651-67404701	U87	brain:	n/a
4	chr8:67380613-67380663	HRCEpiC	kidney:	n/a
5	chr8:67405257-67405307	T-47D	breast:	n/a
6	chr8:67405742-67405792	BE2_C	brain:	n/a
7	chr8:67406954-67407004	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:67405484-67405534	LNCaP	prostate:	n/a
9	chr8:67406954-67407004	HEEpiC	esophagus:	n/a
10	chr8:67380613-67380663	MCF10A-Er-Src	breast:	n/a
11	chr8:67384873-67384923	PANC-1	pancreas:	n/a
12	chr8:67384873-67384923	PFSK-1	brain:	n/a
13	chr8:67380613-67380663	RPTEC	kidney:	n/a
14	chr8:67405405-67405455	AG09309	skin:	n/a
15	chr8:67405405-67405455	Caco-2	colon:	n/a
16	chr8:67405742-67405792	NHBE	bronchial:	n/a
17	chr8:67405405-67405455	NHBE	bronchial:	n/a
18	chr8:67405484-67405534	GM12878	blood:	n/a
19	chr8:67406954-67407004	NH-A	brain:	n/a
20	chr8:67406954-67407004	U87	brain:	n/a
21	chr8:67401313-67401363	U87	brain:	n/a
22	chr8:67405257-67405307	HCT-116	colon:	n/a
23	chr8:67405405-67405455	NH-A	brain:	n/a
24	chr8:67405484-67405534	GM12891	blood:	n/a
25	chr8:67406954-67407004	NT2-D1	testis:	n/a
26	chr8:67405742-67405792	PrEC	prostate:	n/a
27	chr8:67404651-67404701	AG09319	gingival:	n/a
28	chr8:67405484-67405534	CMK	blood:	n/a
29	chr8:67384873-67384923	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:67406954-67407004	ovcar-3	ovarian:	n/a
31	chr8:67401313-67401363	PrEC	prostate:	n/a
32	chr8:67405405-67405455	GM12892	blood:	n/a
33	chr8:67380613-67380663	SK-N-MC	brain:	n/a
34	chr8:67405742-67405792	U87	brain:	n/a
35	chr8:67401313-67401363	HMEC	breast:	n/a
36	chr8:67405742-67405792	HCT-116	colon:	n/a
37	chr8:67405742-67405792	HRPEpiC	eye:	n/a
38	chr8:67405405-67405455	T-47D	breast:	n/a
39	chr8:67384873-67384923	HUVEC	blood vessel:	n/a
40	chr8:67384873-67384923	IMR90	lung:	fetal
41	chr8:67380613-67380663	HCPEpiC	choroid plexus:	n/a
42	chr8:67404651-67404701	PrEC	prostate:	n/a
43	chr8:67405405-67405455	PFSK-1	brain:	n/a
44	chr8:67405484-67405534	HRE	kidney:	n/a
45	chr8:67380613-67380663	NB4	blood:	n/a
46	chr8:67406954-67407004	AG04450	lung:	fetal
47	chr8:67405742-67405792	AG10803	skin:	n/a
48	chr8:67406954-67407004	AG10803	skin:	n/a
49	chr8:67405405-67405455	NT2-D1	testis:	n/a
50	chr8:67384873-67384923	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67378110..67380525-chr8:67519992..67522222,2	MCF-7	breast:
2	chr8:67383309..67385950-chr8:67398891..67400480,2	MCF-7	breast:
3	chr8:67399013..67400552-chr8:67401503..67403129,2	MCF-7	breast:
4	chr8:67401130..67402872-chr8:67415894..67418363,2	K562	blood:
5	chr16:731520..732080-chr8:67384069..67384716,2	HCT-116	colon:
6	chr8:67370426..67372835-chr8:67375511..67377950,2	K562	blood:
7	chr8:67385031..67386596-chr8:67579677..67581320,2	K562	blood:
8	chr16:729976..731206-chr8:67384019..67385398,14	HCT-116	colon:
9	chr8:67401678..67404150-chr8:67442018..67444245,2	K562	blood:
10	chr8:67400231..67403065-chr8:67433723..67435649,2	MCF-7	breast:
11	chr8:67379259..67381817-chr8:67625879..67628203,2	MCF-7	breast:
12	chr8:67387606..67389202-chr8:67836916..67838423,2	MCF-7	breast:
13	chr8:67385468..67387907-chr8:67392199..67395140,2	K562	blood:
14	chr8:67378228..67380679-chr8:67388244..67390416,2	MCF-7	breast:
15	chr8:67378228..67380679-chr8:67388244..67390416,2	MCF-7	breast:
16	chr8:67373363..67378961-chr8:67380708..67384244,6	MCF-7	breast:
17	chr8:67385020..67386788-chr8:67389859..67392152,2	MCF-7	breast:
18	chr17:57920618..57922939-chr8:67379137..67382122,2	MCF-7	breast:
19	chr8:67385468..67387907-chr8:67392199..67395140,2	K562	blood:
20	chr8:67398115..67399973-chr8:67424030..67426495,2	MCF-7	breast:
21	chr8:67399013..67400552-chr8:67401503..67403129,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADHFE1-1	chr8:67385661-67386173	XLOC_006828
2	lnc-ADHFE1-1	chr8:67406779-67407256	NONHSAT127033
3	lnc-ADHFE1-1	chr8:67383684-67383853	XLOC_006828
4	lnc-ADHFE1-1	chr8:67386021-67386173	XLOC_006828
5	lnc-ADHFE1-2	chr8:67392883-67393721	NONHSAT127031
6	lnc-ADHFE1-1	chr8:67405785-67405953	NONHSAT127032
7	lnc-ADHFE1-1	chr8:67387028-67387240	XLOC_006828
8	lnc-ADHFE1-1	chr8:67387028-67387496	XLOC_006828

No data

Variant related genes	Relation type
ENSG00000253623	TF binding region
C8orf46	TF binding region
ENSG00000253623	CpG island
C8orf46	CpG island
ENSG00000270024	chromatin interactions
ENSG00000253623	chromatin interactions
ENSG00000147576	chromatin interactions
ENSG00000169085	chromatin interactions
ENSG00000103266	chromatin interactions
ENSG00000245910	chromatin interactions
ENSG00000213865	chromatin interactions
LCOR	miRNA target sites

Extended variants
information (count: 1185 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11780639	chr8:67376420-67376421	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558023511	chr8:67376434-67376435	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs193202876	chr8:67376516-67376517	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs574081605	chr8:67376559-67376560	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573730945	chr8:67376584-67376585	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs151132222	chr8:67376590-67376591	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369460114	chr8:67376591-67376592	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531833442	chr8:67376653-67376654	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs578158928	chr8:67376689-67376690	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543999478	chr8:67376768-67376769	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565488511	chr8:67376875-67376876	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs141861409	chr8:67376900-67376901	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548139487	chr8:67377050-67377051	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563704294	chr8:67377094-67377095	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182863624	chr8:67377100-67377101	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377045770	chr8:67377104-67377105	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs55731418	chr8:67377124-67377125	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs76753915	chr8:67377132-67377133	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs537956266	chr8:67377133-67377134	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557635271	chr8:67377153-67377154	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs544235923	chr8:67377260-67377261	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577794024	chr8:67377313-67377314	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115333291	chr8:67377322-67377323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75339509	chr8:67377355-67377356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs75644818	chr8:67377376-67377377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187053405	chr8:67377404-67377405	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs2718999	chr8:67377417-67377418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs542563538	chr8:67377418-67377419	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs562908009	chr8:67377421-67377422	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs80285123	chr8:67377428-67377429	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs576423318	chr8:67377456-67377457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs67433773	chr8:67377510-67377511	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs75295460	chr8:67377601-67377602	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564211949	chr8:67377660-67377661	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs191502934	chr8:67377665-67377666	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370366414	chr8:67377668-67377669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541739723	chr8:67377690-67377691	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528485103	chr8:67377782-67377783	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145655143	chr8:67377822-67377823	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533287766	chr8:67377859-67377860	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183694569	chr8:67377920-67377921	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551757515	chr8:67377980-67377981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568852674	chr8:67377985-67377986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147729318	chr8:67377995-67377996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188017378	chr8:67378010-67378011	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374483194	chr8:67378072-67378073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549684141	chr8:67378080-67378081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530687441	chr8:67378084-67378085	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs553550517	chr8:67378086-67378087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567179463	chr8:67378090-67378091	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67359400-67384400	Weak transcription	Fetal Kidney	kidney
2	chr8:67361400-67377400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:67364600-67378800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr8:67364800-67384000	Weak transcription	Colon Smooth Muscle	Colon
5	chr8:67365200-67377400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr8:67365400-67383800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr8:67365800-67379600	Weak transcription	Esophagus	oesophagus
8	chr8:67366000-67376600	Weak transcription	Right Atrium	heart
9	chr8:67368400-67384400	Weak transcription	Psoas Muscle	Psoas
10	chr8:67370800-67384200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr8:67371200-67383800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:67371400-67384200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:67372000-67376800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:67372200-67377600	Strong transcription	Adipose Nuclei	Adipose
15	chr8:67372400-67377000	Strong transcription	Ovary	ovary
16	chr8:67372400-67378800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr8:67372600-67377800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr8:67372600-67381000	Strong transcription	Skeletal Muscle Female	skeletal muscle
19	chr8:67372600-67383600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr8:67372800-67378200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:67372800-67380200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr8:67372800-67381400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:67372800-67383600	Weak transcription	Brain Hippocampus Middle	brain
24	chr8:67372800-67384400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:67372800-67395200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:67373000-67384400	Weak transcription	Brain Angular Gyrus	brain
27	chr8:67373200-67376800	Strong transcription	Brain Cingulate Gyrus	brain
28	chr8:67373400-67377200	Strong transcription	Brain Substantia Nigra	brain
29	chr8:67373600-67380400	Weak transcription	Fetal Muscle Leg	muscle
30	chr8:67373800-67379800	Weak transcription	Gastric	stomach
31	chr8:67373800-67385400	Weak transcription	Fetal Intestine Small	intestine
32	chr8:67374000-67376800	Genic enhancers	Placenta	Placenta
33	chr8:67374000-67379200	Weak transcription	Brain Anterior Caudate	brain
34	chr8:67374000-67381200	Weak transcription	Spleen	Spleen
35	chr8:67374400-67376800	Genic enhancers	Liver	Liver
36	chr8:67374400-67382200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:67374800-67379400	Weak transcription	Aorta	Aorta
38	chr8:67374800-67384600	Weak transcription	Lung	lung
39	chr8:67374800-67396800	Weak transcription	Pancreas	Pancrea
40	chr8:67375000-67379600	Weak transcription	Fetal Intestine Large	intestine
41	chr8:67375000-67384600	Weak transcription	Right Ventricle	heart
42	chr8:67375200-67376800	Enhancers	NHDF-Ad	bronchial
43	chr8:67375200-67376800	Enhancers	Osteobl	bone
44	chr8:67375200-67379000	Weak transcription	Left Ventricle	heart
45	chr8:67375400-67376600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:67375400-67376600	Enhancers	HUVEC	blood vessel
47	chr8:67375400-67376600	Enhancers	NHLF	lung
48	chr8:67375400-67376800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:67375400-67376800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr8:67375400-67376800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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