Variant report

Variant	esv1803798
Chromosome Location	chr8:103974458-103987922
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	chr8:103981045-103981208	HepG2	liver:	n/a	n/a
2	CEBPB	chr8:103976353-103976601	HepG2	liver:	n/a	chr8:103976486-103976497
3	CEBPB	chr8:103976361-103976593	Hela-S3	cervix:	n/a	chr8:103976486-103976497
4	CEBPB	chr8:103976354-103976655	IMR90	lung:	n/a	chr8:103976486-103976497
5	CEBPB	chr8:103976382-103976664	A549	lung:	n/a	chr8:103976486-103976497
6	CTCF	chr8:103982160-103982310	HepG2	liver:	n/a	n/a
7	EP300	chr8:103980859-103981153	SK-N-SH_RA	brain:	n/a	n/a
8	EP300	chr8:103980807-103981171	SK-N-SH_RA	brain:	n/a	n/a
9	FOXA1	chr8:103980917-103981278	HepG2	liver:	n/a	chr8:103981100-103981115 chr8:103981098-103981110
10	FOXA1	chr8:103980844-103981297	HepG2	liver:	n/a	chr8:103981100-103981115 chr8:103981098-103981110
11	FOXA1	chr8:103980920-103981225	HepG2	liver:	n/a	chr8:103981100-103981115 chr8:103981098-103981110
12	FOXA1	chr8:103980845-103981302	HepG2	liver:	n/a	chr8:103981100-103981115 chr8:103981098-103981110
13	FOXA2	chr8:103980776-103981495	HepG2	liver:	n/a	chr8:103981098-103981110
14	FOXA2	chr8:103980933-103981235	HepG2	liver:	n/a	chr8:103981098-103981110
15	JUN	chr8:103976371-103976480	HepG2	liver:	n/a	n/a
16	MAFF	chr8:103985266-103985639	HepG2	liver:	n/a	chr8:103985445-103985463 chr8:103985444-103985458
17	MAFF	chr8:103980871-103981051	HepG2	liver:	n/a	chr8:103980967-103980985
18	MAFF	chr8:103985263-103985649	K562	blood:	n/a	chr8:103985445-103985463 chr8:103985444-103985458
19	MAFK	chr8:103985263-103985687	HepG2	liver:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
20	MAFK	chr8:103985261-103985730	GM12878	blood:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
21	MAFK	chr8:103981016-103981041	HepG2	liver:	n/a	n/a
22	MAFK	chr8:103985273-103985638	H1-hESC	embryonic stem cell:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
23	MAFK	chr8:103985270-103985640	K562	blood:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
24	MAFK	chr8:103985279-103985686	Hela-S3	cervix:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
25	MAFK	chr8:103985256-103985719	IMR90	lung:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
26	MAFK	chr8:103985271-103985637	HepG2	liver:	n/a	chr8:103985444-103985458 chr8:103985441-103985461 chr8:103985446-103985461 chr8:103985446-103985462 chr8:103985443-103985459
27	MAX	chr8:103985446-103985725	NB4	blood:	n/a	n/a
28	MXI1	chr8:103980602-103981346	SK-N-SH	brain:	n/a	n/a
29	MYC	chr8:103985495-103985682	NB4	blood:	n/a	n/a
30	NR2F2	chr8:103979093-103979568	MCF-7	breast:	n/a	n/a
31	POLR2A	chr8:103975899-103975931	MCF10A-Er-Src	breast:	n/a	n/a
32	SPI1	chr8:103986247-103986401	K562	blood:	n/a	n/a
33	SPI1	chr8:103986244-103986465	GM12891	blood:	n/a	n/a
34	SPI1	chr8:103985352-103985810	HL-60	blood:	n/a	n/a
35	SPI1	chr8:103983093-103983476	HL-60	blood:	n/a	n/a
36	STAT3	chr8:103980614-103980707	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr8:103985652-103985715	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr8:103977858-103977879	MCF10A-Er-Src	breast:	n/a	n/a
39	TEAD4	chr8:103976863-103977260	H1-hESC	embryonic stem cell:	n/a	n/a
40	ZNF217	chr8:103979064-103979644	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103981066-103981116	NHDF-neo	bronchial:	n/a
2	chr8:103981066-103981116	SK-N-SH_RA	brain:	n/a
3	chr8:103981066-103981116	HCT-116	colon:	n/a
4	chr8:103981066-103981116	HEK293	kidney:	embryo
5	chr8:103981066-103981116	PFSK-1	brain:	n/a
6	chr8:103981066-103981116	HIPEpiC	eye:	n/a
7	chr8:103981066-103981116	Caco-2	colon:	n/a
8	chr8:103981066-103981116	AG04450	lung:	fetal
9	chr8:103981066-103981116	GM12892	blood:	n/a
10	chr8:103981066-103981116	K562	blood:	n/a
11	chr8:103981066-103981116	GM19239	blood:	n/a
12	chr8:103981066-103981116	HRCEpiC	kidney:	n/a
13	chr8:103981066-103981116	U87	brain:	n/a
14	chr8:103981066-103981116	MCF10A-Er-Src	breast:	n/a
15	chr8:103981066-103981116	HMEC	breast:	n/a
16	chr8:103981066-103981116	SK-N-SH	brain:	n/a
17	chr8:103981066-103981116	IMR90	lung:	fetal
18	chr8:103981066-103981116	GM12878	blood:	n/a
19	chr8:103981066-103981116	MCF-7	breast:	n/a
20	chr8:103981066-103981116	HUVEC	blood vessel:	n/a
21	chr8:103981066-103981116	AG09319	gingival:	n/a
22	chr8:103981066-103981116	BJ	skin:	n/a
23	chr8:103981066-103981116	PrEC	prostate:	n/a
24	chr8:103981066-103981116	HNPCEpiC	eye:	n/a
25	chr8:103981066-103981116	ECC-1	luminal epithelium:	n/a
26	chr8:103981066-103981116	LNCaP	prostate:	n/a
27	chr8:103981066-103981116	HRE	kidney:	n/a
28	chr8:103981066-103981116	NT2-D1	testis:	n/a
29	chr8:103981066-103981116	SKMC	muscle:	n/a
30	chr8:103981066-103981116	SAEC	small airway:	n/a
31	chr8:103981066-103981116	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:103981066-103981116	HL-60	blood:	n/a
33	chr8:103981066-103981116	HEEpiC	esophagus:	n/a
34	chr8:103981066-103981116	AoSMC	blood vessel:	n/a
35	chr8:103981066-103981116	PANC-1	pancreas:	n/a
36	chr8:103981066-103981116	NH-A	brain:	n/a
37	chr8:103981066-103981116	HCM	heart:	n/a
38	chr8:103981066-103981116	ovcar-3	ovarian:	n/a
39	chr8:103981066-103981116	BE2_C	brain:	n/a
40	chr8:103981066-103981116	NB4	blood:	n/a
41	chr8:103981066-103981116	Hela-S3	cervix:	n/a
42	chr8:103981066-103981116	HAEpiC	amniotic membrane:	n/a
43	chr8:103981066-103981116	ProgFib	skin:	n/a
44	chr8:103981066-103981116	CMK	blood:	n/a
45	chr8:103981066-103981116	AG04449	skin:	fetal
46	chr8:103981066-103981116	SK-N-MC	brain:	n/a
47	chr8:103981066-103981116	GM06990	blood:	n/a
48	chr8:103981066-103981116	A549	lung:	n/a
49	chr8:103981066-103981116	H1-hESC	embryonic stem cell:	embryo
50	chr8:103981066-103981116	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:103979381..103981672-chr8:103986062..103989018,2	MCF-7	breast:
2	chr8:103979381..103981672-chr8:103986062..103989018,2	MCF-7	breast:
3	chr8:103984545..103986132-chr8:103993005..103995689,2	MCF-7	breast:
4	chr8:103874838..103876433-chr8:103978031..103981018,2	MCF-7	breast:
5	chr8:103977894..103979426-chr8:103982268..103984695,2	MCF-7	breast:
6	chr8:103987503..103990254-chr8:104000739..104004845,3	MCF-7	breast:
7	chr8:103987556..103990076-chr8:103994687..103996398,2	K562	blood:
8	chr8:103874782..103876316-chr8:103973931..103975682,2	MCF-7	breast:
9	chr8:103875112..103879316-chr8:103972204..103974673,4	MCF-7	breast:
10	chr8:103977894..103979426-chr8:103982268..103984695,2	MCF-7	breast:
11	chr8:103874330..103878583-chr8:103978201..103983603,5	MCF-7	breast:
12	chr8:103983197..103984715-chr8:103998535..104001425,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1507C5.2.1-4	chr8:103984549-103984599	NONHSAT128139
2	lnc-KB-1507C5.2.1-4	chr8:103979765-103979901	NONHSAT128141
3	lnc-KB-1507C5.2.1-4	chr8:103979825-103979901	NONHSAT128122
4	lnc-ATP6V1C1-6	chr8:103976074-103976692	ncRnaDb_ncrna_FR026950_1

Variant related genes	Relation type
ENSG00000265898	TF binding region
ENSG00000254281	TF binding region
ENSG00000265898	CpG island
ENSG00000254281	CpG island
ENSG00000253320	chromatin interactions
ENSG00000155096	chromatin interactions

Extended variants
information (count: 533 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:533 , 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	rs7003697	chr8:103974458-103974459	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565240948	chr8:103974471-103974472	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs553792165	chr8:103974488-103974489	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372904280	chr8:103974539-103974540	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77567632	chr8:103974547-103974548	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562578553	chr8:103974579-103974580	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs60254080	chr8:103974592-103974593	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146308129	chr8:103974617-103974618	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191873709	chr8:103974630-103974631	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs34149592	chr8:103974686-103974687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528283010	chr8:103974713-103974714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs546626943	chr8:103974725-103974726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183690978	chr8:103974787-103974788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538775977	chr8:103974840-103974841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573698263	chr8:103974849-103974850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368877612	chr8:103974918-103974919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566675823	chr8:103974930-103974931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568897707	chr8:103974946-103974947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536916429	chr8:103974958-103974959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536202058	chr8:103974970-103974971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533782837	chr8:103974991-103974992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139035477	chr8:103975032-103975033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573342311	chr8:103975051-103975052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188359148	chr8:103975061-103975062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141640190	chr8:103975074-103975075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577251512	chr8:103975148-103975149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs556396956	chr8:103975152-103975153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562515978	chr8:103975172-103975173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373483386	chr8:103975183-103975184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114218923	chr8:103975189-103975190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs375826412	chr8:103975192-103975193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181804849	chr8:103975202-103975203	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561027385	chr8:103975215-103975216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140417791	chr8:103975221-103975222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370805416	chr8:103975222-103975223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs60704553	chr8:103975233-103975234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1714397	chr8:103975259-103975260	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369747030	chr8:103975269-103975270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541814294	chr8:103975315-103975316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7837635	chr8:103975325-103975326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550715271	chr8:103975331-103975332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558014417	chr8:103975338-103975339	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141272817	chr8:103975369-103975370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs111795292	chr8:103975396-103975397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536258286	chr8:103975413-103975414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs578028562	chr8:103975484-103975485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187414255	chr8:103975507-103975508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs534542940	chr8:103975515-103975516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558862868	chr8:103975544-103975545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577046179	chr8:103975587-103975588	Weak transcription	Chromatin interactive region	1 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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103973200-103975200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:103973400-103974600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:103973400-103974600	Enhancers	Brain Hippocampus Middle	brain
4	chr8:103973400-103974800	Enhancers	Thymus	Thymus
5	chr8:103973400-103974800	Enhancers	GM12878-XiMat	blood
6	chr8:103973400-103975000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:103973600-103974600	Enhancers	Brain Substantia Nigra	brain
8	chr8:103973600-103974600	Enhancers	HSMM	muscle
9	chr8:103973600-103974800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:103973600-103974800	Enhancers	Fetal Kidney	kidney
11	chr8:103973600-103975000	Enhancers	Brain Cingulate Gyrus	brain
12	chr8:103973600-103975400	Enhancers	Fetal Thymus	thymus
13	chr8:103973800-103974800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:103973800-103974800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:103974000-103974600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:103974000-103978000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr8:103974200-103974600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:103974200-103974800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr8:103974200-103977600	Weak transcription	Adipose Nuclei	Adipose
20	chr8:103974200-103977800	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr8:103974200-103977800	Weak transcription	Brain Anterior Caudate	brain
22	chr8:103974200-103979800	Weak transcription	Fetal Muscle Leg	muscle
23	chr8:103974400-103976000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr8:103974400-103976000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr8:103974400-103976000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr8:103974400-103976000	Weak transcription	Placenta	Placenta
27	chr8:103974400-103976000	Weak transcription	Ovary	ovary
28	chr8:103974400-103976000	Weak transcription	Pancreas	Pancrea
29	chr8:103974400-103976200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr8:103974400-103976400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr8:103974400-103977800	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr8:103974400-103979400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:103974400-103980400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr8:103974400-103980800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:103974400-103989200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr8:103974400-103989200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:103974600-103976000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr8:103974800-103976000	Weak transcription	Fetal Kidney	kidney
39	chr8:103974800-103976000	Weak transcription	Thymus	Thymus
40	chr8:103974800-103976200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr8:103974800-103978600	Weak transcription	Right Atrium	heart
42	chr8:103974800-103982200	Weak transcription	GM12878-XiMat	blood
43	chr8:103975000-103980400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr8:103975400-103975800	Weak transcription	Fetal Thymus	thymus
45	chr8:103975800-103976200	Enhancers	Fetal Thymus	thymus
46	chr8:103976000-103976400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr8:103976000-103976400	Enhancers	Fetal Stomach	stomach
48	chr8:103976000-103976400	Enhancers	Ovary	ovary
49	chr8:103976000-103976400	Enhancers	Pancreas	Pancrea
50	chr8:103976000-103976800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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