Variant report

Variant	nsv611457
Chromosome Location	chr8:67375519-67385088
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:281)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:67376527-67376760	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:67375399-67376000	HepG2	liver:	n/a	chr8:67375704-67375720 chr8:67375703-67375719
3	BRCA1	chr8:67383595-67383967	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr8:67383537-67383999	HCT-116	colon:	n/a	n/a
5	CEBPB	chr8:67383127-67383379	A549	lung:	n/a	n/a
6	CEBPB	chr8:67383582-67383903	A549	lung:	n/a	n/a
7	CEBPB	chr8:67383447-67384093	A549	lung:	n/a	n/a
8	CEBPB	chr8:67383574-67383955	IMR90	lung:	n/a	n/a
9	CEBPB	chr8:67384997-67385194	A549	lung:	n/a	chr8:67385137-67385148
10	CEBPB	chr8:67376884-67377099	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:67375426-67376095	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr8:67376696-67377167	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:67375578-67376146	A549	lung:	n/a	n/a
14	CEBPB	chr8:67384973-67385233	K562	blood:	n/a	chr8:67385137-67385148
15	CEBPB	chr8:67383544-67383955	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:67385016-67385148	H1-hESC	embryonic stem cell:	n/a	chr8:67385137-67385148
17	CEBPB	chr8:67375764-67376104	IMR90	lung:	n/a	n/a
18	CHD2	chr8:67384509-67384728	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:67379220-67379370	HMF	breast:	n/a	n/a
20	CTCF	chr8:67379223-67379382	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:67379200-67379350	HepG2	liver:	n/a	n/a
22	CTCF	chr8:67379280-67379430	HCT-116	colon:	n/a	n/a
23	CTCF	chr8:67379180-67379330	AG09309	skin:	n/a	n/a
24	CTCF	chr8:67379260-67379410	HVMF	connective:	n/a	n/a
25	CTCF	chr8:67379180-67379330	GM12871	blood:	n/a	n/a
26	CTCF	chr8:67379303-67379373	GM12891	blood:	n/a	n/a
27	CTCF	chr8:67379260-67379410	GM12873	blood:	n/a	n/a
28	CTCF	chr8:67379160-67379310	BJ	skin:	n/a	n/a
29	CTCF	chr8:67379160-67379310	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr8:67379240-67379390	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr8:67379140-67379290	BE2_C	brain:	n/a	n/a
32	CTCF	chr8:67379220-67379370	AG10803	skin:	n/a	n/a
33	CTCF	chr8:67379270-67379373	GM19238	blood:	n/a	n/a
34	CTCF	chr8:67379200-67379350	GM12873	blood:	n/a	n/a
35	CTCF	chr8:67379180-67379330	HRE	kidney:	n/a	n/a
36	CTCF	chr8:67379280-67379430	Caco-2	colon:	n/a	n/a
37	CTCF	chr8:67379278-67379343	NHEK	skin:	n/a	n/a
38	CTCF	chr8:67379160-67379310	GM06990	blood:	n/a	n/a
39	CTCF	chr8:67379220-67379370	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr8:67379142-67379452	GM12878	blood:	n/a	n/a
41	CTCF	chr8:67379240-67379390	AG10803	skin:	n/a	n/a
42	CTCF	chr8:67379100-67379250	HMF	breast:	n/a	n/a
43	CTCF	chr8:67379200-67379350	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr8:67379200-67379350	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:67379200-67379350	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr8:67379240-67379390	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr8:67379280-67379570	GM12872	blood:	n/a	n/a
48	CTCF	chr8:67379140-67379290	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr8:67379240-67379390	Caco-2	colon:	n/a	n/a
50	CTCF	chr8:67379242-67379408	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67380613-67380663	HIPEpiC	eye:	n/a
2	chr8:67384873-67384923	Hepatocyte	liver:	n/a
3	chr8:67380613-67380663	MCF10A-Er-Src	breast:	n/a
4	chr8:67384873-67384923	RPTEC	kidney:	n/a
5	chr8:67384873-67384923	SK-N-MC	brain:	n/a
6	chr8:67384873-67384923	NHDF-neo	bronchial:	n/a
7	chr8:67380613-67380663	PANC-1	pancreas:	n/a
8	chr8:67380613-67380663	NB4	blood:	n/a
9	chr8:67380613-67380663	PrEC	prostate:	n/a
10	chr8:67380613-67380663	PFSK-1	brain:	n/a
11	chr8:67380613-67380663	GM12878	blood:	n/a
12	chr8:67380613-67380663	IMR90	lung:	fetal
13	chr8:67380613-67380663	NHBE	bronchial:	n/a
14	chr8:67384873-67384923	NT2-D1	testis:	n/a
15	chr8:67380613-67380663	HUVEC	blood vessel:	n/a
16	chr8:67384873-67384923	HNPCEpiC	eye:	n/a
17	chr8:67380613-67380663	K562	blood:	n/a
18	chr8:67384873-67384923	CMK	blood:	n/a
19	chr8:67384873-67384923	GM06990	blood:	n/a
20	chr8:67384873-67384923	SK-N-SH	brain:	n/a
21	chr8:67380613-67380663	MCF-7	breast:	n/a
22	chr8:67380613-67380663	Jurkat	blood:	n/a
23	chr8:67384873-67384923	HIPEpiC	eye:	n/a
24	chr8:67380613-67380663	HCM	heart:	n/a
25	chr8:67380613-67380663	NH-A	brain:	n/a
26	chr8:67380613-67380663	U87	brain:	n/a
27	chr8:67380613-67380663	HRPEpiC	eye:	n/a
28	chr8:67384873-67384923	ProgFib	skin:	n/a
29	chr8:67380613-67380663	A549	lung:	n/a
30	chr8:67384873-67384923	ECC-1	luminal epithelium:	n/a
31	chr8:67384873-67384923	AG10803	skin:	n/a
32	chr8:67384873-67384923	HEEpiC	esophagus:	n/a
33	chr8:67380613-67380663	HEEpiC	esophagus:	n/a
34	chr8:67384873-67384923	HCM	heart:	n/a
35	chr8:67384873-67384923	Jurkat	blood:	n/a
36	chr8:67384873-67384923	NB4	blood:	n/a
37	chr8:67380613-67380663	CMK	blood:	n/a
38	chr8:67384873-67384923	AG09319	gingival:	n/a
39	chr8:67384873-67384923	NHBE	bronchial:	n/a
40	chr8:67380613-67380663	HepG2	liver:	n/a
41	chr8:67380613-67380663	GM12891	blood:	n/a
42	chr8:67384873-67384923	A549	lung:	n/a
43	chr8:67380613-67380663	NT2-D1	testis:	n/a
44	chr8:67384873-67384923	IMR90	lung:	fetal
45	chr8:67380613-67380663	BJ	skin:	n/a
46	chr8:67380613-67380663	AoSMC	blood vessel:	n/a
47	chr8:67384873-67384923	HRCEpiC	kidney:	n/a
48	chr8:67384873-67384923	NH-A	brain:	n/a
49	chr8:67384873-67384923	HepG2	liver:	n/a
50	chr8:67380613-67380663	BE2_C	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67385031..67386596-chr8:67579677..67581320,2	K562	blood:
2	chr8:67374151..67375671-chr8:67623910..67626033,2	MCF-7	breast:
3	chr8:67370426..67372835-chr8:67375511..67377950,2	K562	blood:
4	chr16:729976..731206-chr8:67384019..67385398,14	HCT-116	colon:
5	chr8:67373454..67375848-chr8:67443609..67445864,2	MCF-7	breast:
6	chr8:67378110..67380525-chr8:67519992..67522222,2	MCF-7	breast:
7	chr8:67371423..67376205-chr8:67520601..67527002,8	MCF-7	breast:
8	chr8:67373363..67378961-chr8:67380708..67384244,6	MCF-7	breast:
9	chr16:731520..732080-chr8:67384069..67384716,2	HCT-116	colon:
10	chr17:57920618..57922939-chr8:67379137..67382122,2	MCF-7	breast:
11	chr8:67379259..67381817-chr8:67625879..67628203,2	MCF-7	breast:
12	chr8:67378228..67380679-chr8:67388244..67390416,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADHFE1-1	chr8:67383684-67383853	XLOC_006828

No data

Variant related genes	Relation type
C8orf46	TF binding region
C8orf46	CpG island
ENSG00000147576	chromatin interactions
ENSG00000213865	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000169085	chromatin interactions
ENSG00000185697	chromatin interactions
ENSG00000270024	chromatin interactions
ENSG00000103266	chromatin interactions

Extended variants
information (count: 352 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2555575	chr8:67375519-67375520	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146245031	chr8:67375608-67375609	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs377097553	chr8:67375629-67375630	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs2718998	chr8:67375638-67375639	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs540189774	chr8:67375658-67375659	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs560125340	chr8:67375659-67375660	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs529319577	chr8:67375663-67375664	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs192026328	chr8:67375727-67375728	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs112981327	chr8:67375736-67375737	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs554157088	chr8:67375793-67375794	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs57960361	chr8:67375842-67375843	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549093482	chr8:67375847-67375848	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs151023301	chr8:67375853-67375854	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs398067900	chr8:67375854-67375855	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs139301346	chr8:67375927-67375928	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531849081	chr8:67375956-67375957	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552044989	chr8:67375989-67375990	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs78348791	chr8:67376001-67376002	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs149915757	chr8:67376017-67376018	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs539623891	chr8:67376115-67376116	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs534514719	chr8:67376134-67376135	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs201873377	chr8:67376139-67376140	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs146433998	chr8:67376155-67376156	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183908837	chr8:67376194-67376195	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs144939974	chr8:67376195-67376196	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs148630332	chr8:67376242-67376243	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535523956	chr8:67376280-67376281	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555538501	chr8:67376294-67376295	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575387462	chr8:67376356-67376357	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs188705904	chr8:67376377-67376378	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142069239	chr8:67376390-67376391	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	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
33	rs558023511	chr8:67376434-67376435	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs193202876	chr8:67376516-67376517	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574081605	chr8:67376559-67376560	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs573730945	chr8:67376584-67376585	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs151132222	chr8:67376590-67376591	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369460114	chr8:67376591-67376592	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531833442	chr8:67376653-67376654	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs578158928	chr8:67376689-67376690	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543999478	chr8:67376768-67376769	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs565488511	chr8:67376875-67376876	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141861409	chr8:67376900-67376901	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548139487	chr8:67377050-67377051	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563704294	chr8:67377094-67377095	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs182863624	chr8:67377100-67377101	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs377045770	chr8:67377104-67377105	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs55731418	chr8:67377124-67377125	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs76753915	chr8:67377132-67377133	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537956266	chr8:67377133-67377134	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 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:314 , 50 per page) page: 1 2 3 4 5 6 7

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	chr8:67364400-67375800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr8:67364600-67378800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr8:67364800-67384000	Weak transcription	Colon Smooth Muscle	Colon
6	chr8:67365200-67377400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr8:67365400-67383800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr8:67365800-67379600	Weak transcription	Esophagus	oesophagus
9	chr8:67366000-67376600	Weak transcription	Right Atrium	heart
10	chr8:67368400-67384400	Weak transcription	Psoas Muscle	Psoas
11	chr8:67369000-67375800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:67369000-67376000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:67369000-67376000	Weak transcription	Fetal Heart	heart
14	chr8:67370800-67384200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:67371200-67383800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:67371400-67384200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:67372000-67376800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:67372200-67377600	Strong transcription	Adipose Nuclei	Adipose
19	chr8:67372400-67375600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:67372400-67375800	Weak transcription	NHEK	skin
21	chr8:67372400-67377000	Strong transcription	Ovary	ovary
22	chr8:67372400-67378800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:67372600-67375600	Weak transcription	HMEC	breast
24	chr8:67372600-67377800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:67372600-67381000	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr8:67372600-67383600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:67372800-67375800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:67372800-67378200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr8:67372800-67380200	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr8:67372800-67381400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:67372800-67383600	Weak transcription	Brain Hippocampus Middle	brain
32	chr8:67372800-67384400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:67372800-67395200	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr8:67373000-67384400	Weak transcription	Brain Angular Gyrus	brain
35	chr8:67373200-67376800	Strong transcription	Brain Cingulate Gyrus	brain
36	chr8:67373400-67377200	Strong transcription	Brain Substantia Nigra	brain
37	chr8:67373600-67376000	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr8:67373600-67380400	Weak transcription	Fetal Muscle Leg	muscle
39	chr8:67373800-67375600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr8:67373800-67376000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:67373800-67379800	Weak transcription	Gastric	stomach
42	chr8:67373800-67385400	Weak transcription	Fetal Intestine Small	intestine
43	chr8:67374000-67375600	Weak transcription	Fetal Stomach	stomach
44	chr8:67374000-67376800	Genic enhancers	Placenta	Placenta
45	chr8:67374000-67379200	Weak transcription	Brain Anterior Caudate	brain
46	chr8:67374000-67381200	Weak transcription	Spleen	Spleen
47	chr8:67374400-67376800	Genic enhancers	Liver	Liver
48	chr8:67374400-67382200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr8:67374800-67375600	Enhancers	A549	lung
50	chr8:67374800-67375800	Enhancers	Stomach Smooth Muscle	stomach

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