Variant report

Variant	esv1798999
Chromosome Location	chr8:96498811-96518612
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	CTCF	chr8:96515700-96515850	HMEC	breast:	n/a	chr8:96515820-96515833
2	CTCF	chr8:96515740-96515890	Caco-2	colon:	n/a	chr8:96515820-96515833
3	CTCF	chr8:96515773-96515837	Lung_OC	lung:	n/a	chr8:96515820-96515833
4	CTCF	chr8:96515694-96515929	HUVEC	blood vessel:	n/a	chr8:96515820-96515833
5	CTCF	chr8:96515740-96515890	HUVEC	blood vessel:	n/a	chr8:96515820-96515833
6	CTCF	chr8:96515809-96515874	GM12892	blood:	n/a	chr8:96515820-96515833
7	CTCF	chr8:96515780-96515930	GM06990	blood:	n/a	chr8:96515820-96515833
8	CTCF	chr8:96515440-96515590	HAc	cerebellar:	n/a	n/a
9	CTCF	chr8:96515740-96515890	GM12871	blood:	n/a	chr8:96515820-96515833
10	CTCF	chr8:96515700-96515850	SAEC	small airway:	n/a	chr8:96515820-96515833
11	CTCF	chr8:96515740-96515890	HEK293	kidney:	n/a	chr8:96515820-96515833
12	CTCF	chr8:96515777-96515895	MCF-7	breast:	n/a	chr8:96515820-96515833
13	CTCF	chr8:96515763-96515899	Spleen_OC	spleen:	n/a	chr8:96515820-96515833
14	CTCF	chr8:96515780-96515930	HAc	cerebellar:	n/a	chr8:96515820-96515833
15	CTCF	chr8:96515871-96515878	GM12878	blood:	n/a	n/a
16	CTCF	chr8:96515740-96515890	HRE	kidney:	n/a	chr8:96515820-96515833
17	CTCF	chr8:96515700-96515850	HVMF	connective:	n/a	chr8:96515820-96515833
18	CTCF	chr8:96515720-96515870	AG09319	gingival:	n/a	chr8:96515820-96515833
19	CTCF	chr8:96515723-96515934	Fibrobl	skin:	n/a	chr8:96515820-96515833
20	CTCF	chr8:96515718-96515957	GM12878	blood:	n/a	chr8:96515820-96515833
21	CTCF	chr8:96515806-96515837	GM19238	blood:	n/a	chr8:96515820-96515833
22	CTCF	chr8:96515740-96515890	HA-sp	spinal cord:	n/a	chr8:96515820-96515833
23	CTCF	chr8:96515760-96515910	MCF-7	breast:	n/a	chr8:96515820-96515833
24	CTCF	chr8:96515700-96515850	GM12870	blood:	n/a	chr8:96515820-96515833
25	CTCF	chr8:96515740-96515890	HEEpiC	esophagus:	n/a	chr8:96515820-96515833
26	CTCF	chr8:96515720-96515870	HMEC	breast:	n/a	chr8:96515820-96515833
27	CTCF	chr8:96515760-96515910	HPAF	blood vessel:	n/a	chr8:96515820-96515833
28	CTCF	chr8:96515780-96515930	AG04450	lung:	n/a	chr8:96515820-96515833
29	CTCF	chr8:96515720-96515870	HAc	cerebellar:	n/a	chr8:96515820-96515833
30	CTCF	chr8:96515700-96515850	HFF	foreskin:	n/a	chr8:96515820-96515833
31	CTCF	chr8:96515660-96515810	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr8:96515808-96515853	Hela-S3	cervix:	n/a	chr8:96515820-96515833
33	CTCF	chr8:96515731-96515906	MCF-7	breast:	n/a	chr8:96515820-96515833
34	CTCF	chr8:96515780-96515930	RPTEC	kidney:	n/a	chr8:96515820-96515833
35	CTCF	chr8:96515740-96515890	HCPEpiC	choroid plexus:	n/a	chr8:96515820-96515833
36	CTCF	chr8:96515760-96515910	A549	lung:	n/a	chr8:96515820-96515833
37	CTCF	chr8:96515880-96516030	HCM	heart:	n/a	n/a
38	CTCF	chr8:96515760-96515910	AoAF	blood vessel:	n/a	chr8:96515820-96515833
39	CTCF	chr8:96515780-96515930	HRE	kidney:	n/a	chr8:96515820-96515833
40	CTCF	chr8:96515568-96516050	HCT-116	colon:	n/a	chr8:96515820-96515833
41	CTCF	chr8:96515756-96515873	GM10266	blood:	n/a	chr8:96515820-96515833
42	CTCF	chr8:96515800-96515950	NB4	blood:	n/a	chr8:96515820-96515833
43	CTCF	chr8:96515720-96515870	NHDF-neo	bronchial:	n/a	chr8:96515820-96515833
44	CTCF	chr8:96515720-96515870	K562	blood:	n/a	chr8:96515820-96515833
45	CTCF	chr8:96515700-96515850	HA-sp	spinal cord:	n/a	chr8:96515820-96515833
46	CTCF	chr8:96515760-96515910	HCPEpiC	choroid plexus:	n/a	chr8:96515820-96515833
47	CTCF	chr8:96515720-96515870	NHLF	lung:	n/a	chr8:96515820-96515833
48	CTCF	chr8:96515761-96515915	MCF-7	breast:	n/a	chr8:96515820-96515833
49	CTCF	chr8:96515587-96516098	MCF-7	breast:	n/a	chr8:96515820-96515833
50	CTCF	chr8:96515688-96515932	H1-hESC	embryonic stem cell:	n/a	chr8:96515820-96515833

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96504381-96504431	SK-N-SH_RA	brain:	n/a
2	chr8:96504381-96504431	RPTEC	kidney:	n/a
3	chr8:96504381-96504431	Hepatocyte	liver:	n/a
4	chr8:96504381-96504431	HEEpiC	esophagus:	n/a
5	chr8:96504381-96504431	HAEpiC	amniotic membrane:	n/a
6	chr8:96504381-96504431	GM06990	blood:	n/a
7	chr8:96504381-96504431	ECC-1	luminal epithelium:	n/a
8	chr8:96504381-96504431	HMEC	breast:	n/a
9	chr8:96504381-96504431	SK-N-MC	brain:	n/a
10	chr8:96504381-96504431	LNCaP	prostate:	n/a
11	chr8:96504381-96504431	U87	brain:	n/a
12	chr8:96504381-96504431	GM12878	blood:	n/a
13	chr8:96504381-96504431	HUVEC	blood vessel:	n/a
14	chr8:96504381-96504431	HepG2	liver:	n/a
15	chr8:96504381-96504431	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:96504381-96504431	AG09319	gingival:	n/a
17	chr8:96504381-96504431	AG04449	skin:	fetal
18	chr8:96504381-96504431	PFSK-1	brain:	n/a
19	chr8:96504381-96504431	HCPEpiC	choroid plexus:	n/a
20	chr8:96504381-96504431	AG09309	skin:	n/a
21	chr8:96504381-96504431	HRE	kidney:	n/a
22	chr8:96504381-96504431	SK-N-SH	brain:	n/a
23	chr8:96504381-96504431	GM12891	blood:	n/a
24	chr8:96504381-96504431	SKMC	muscle:	n/a
25	chr8:96504381-96504431	IMR90	lung:	fetal
26	chr8:96504381-96504431	PANC-1	pancreas:	n/a
27	chr8:96504381-96504431	AG04450	lung:	fetal
28	chr8:96504381-96504431	ovcar-3	ovarian:	n/a
29	chr8:96504381-96504431	GM12892	blood:	n/a
30	chr8:96504381-96504431	HCF	heart:	n/a
31	chr8:96504381-96504431	HNPCEpiC	eye:	n/a
32	chr8:96504381-96504431	HIPEpiC	eye:	n/a
33	chr8:96504381-96504431	Caco-2	colon:	n/a
34	chr8:96504381-96504431	HRPEpiC	eye:	n/a
35	chr8:96504381-96504431	NH-A	brain:	n/a
36	chr8:96504381-96504431	HCT-116	colon:	n/a
37	chr8:96504381-96504431	AoSMC	blood vessel:	n/a
38	chr8:96504381-96504431	AG10803	skin:	n/a
39	chr8:96504381-96504431	GM19239	blood:	n/a
40	chr8:96504381-96504431	NT2-D1	testis:	n/a
41	chr8:96504381-96504431	BE2_C	brain:	n/a
42	chr8:96504381-96504431	NHBE	bronchial:	n/a
43	chr8:96504381-96504431	Jurkat	blood:	n/a
44	chr8:96504381-96504431	A549	lung:	n/a
45	chr8:96504381-96504431	HL-60	blood:	n/a
46	chr8:96504381-96504431	HEK293	kidney:	embryo
47	chr8:96504381-96504431	Hela-S3	cervix:	n/a
48	chr8:96504381-96504431	SAEC	small airway:	n/a
49	chr8:96504381-96504431	PrEC	prostate:	n/a
50	chr8:96504381-96504431	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:96515360..96516198-chr8:96770656..96771587,2	MCF-7	breast:
2	chr8:96495853..96497993-chr8:96501094..96502749,2	K562	blood:
3	chr13:83085927..83086427-chr8:96515336..96516158,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-1	chr8:96517634-96517853	ENSG00000253872

Variant related genes	Relation type
ENSG00000253872	TF binding region
ENSG00000253872	CpG island

Extended variants
information (count: 489 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16917764	chr8:96498811-96498812	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569215649	chr8:96498848-96498849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181901110	chr8:96498897-96498898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575282342	chr8:96498903-96498904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551842012	chr8:96498906-96498907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145554722	chr8:96498961-96498962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35676077	chr8:96498962-96498963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35579267	chr8:96498963-96498964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184258911	chr8:96499013-96499014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112868110	chr8:96499038-96499039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73274654	chr8:96499050-96499051	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572717283	chr8:96499071-96499072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566309057	chr8:96499125-96499126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546184277	chr8:96499171-96499172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58465747	chr8:96499183-96499184	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs575160922	chr8:96499186-96499187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543920542	chr8:96499202-96499203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376139202	chr8:96499223-96499224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146373636	chr8:96499253-96499254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367741011	chr8:96499254-96499255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577624874	chr8:96499311-96499312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577789704	chr8:96499385-96499386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560644032	chr8:96499417-96499418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565189269	chr8:96499419-96499420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138263602	chr8:96499438-96499439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73697834	chr8:96499479-96499480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547659420	chr8:96499507-96499508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531727058	chr8:96499526-96499527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540004674	chr8:96499530-96499531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533936044	chr8:96499590-96499591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181063958	chr8:96499591-96499592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12549682	chr8:96499611-96499612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573595356	chr8:96499647-96499648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10956953	chr8:96499699-96499700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs566308890	chr8:96499723-96499724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562886666	chr8:96499765-96499766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56314554	chr8:96499795-96499796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555624263	chr8:96499830-96499831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113612181	chr8:96499936-96499937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538152999	chr8:96499942-96499943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs59057318	chr8:96499947-96499948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144388510	chr8:96499997-96499998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565202823	chr8:96500022-96500023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7011173	chr8:96500035-96500036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs147496382	chr8:96500162-96500163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185157073	chr8:96500165-96500166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201057219	chr8:96500172-96500173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574276692	chr8:96500200-96500201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530442101	chr8:96500310-96500311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543288212	chr8:96500329-96500330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96497000-96499200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr8:96497200-96499200	Enhancers	HSMM	muscle
3	chr8:96498400-96504400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:96498800-96499200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr8:96498800-96499400	Enhancers	HSMMtube	muscle
6	chr8:96501400-96502800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:96502800-96503000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:96502800-96503200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:96503000-96505000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:96504000-96505200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:96504000-96505200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:96504000-96505200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:96504200-96504800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:96504200-96505400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:96504200-96505600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:96504400-96505200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:96504400-96506600	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr8:96504800-96506400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr8:96505000-96505200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:96505200-96505800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:96505400-96505800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:96505600-96506000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:96505800-96506000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:96505800-96506600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:96506000-96506400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:96506200-96506800	Enhancers	Fetal Muscle Leg	muscle
27	chr8:96506400-96506600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:96506600-96507000	Enhancers	HSMM	muscle
29	chr8:96510200-96510600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:96510200-96511200	Enhancers	Liver	Liver
31	chr8:96510600-96511000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:96511000-96511800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:96514000-96514800	Enhancers	HUVEC	blood vessel
34	chr8:96514800-96515800	Weak transcription	HUVEC	blood vessel
35	chr8:96515400-96515600	Bivalent Enhancer	Osteobl	bone
36	chr8:96515400-96515800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:96515400-96515800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:96515400-96515800	Enhancers	HSMMtube	muscle
39	chr8:96515400-96516000	Enhancers	Colon Smooth Muscle	Colon
40	chr8:96515400-96516200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr8:96515400-96516200	Enhancers	HSMM	muscle
42	chr8:96515600-96515800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:96515600-96515800	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr8:96515600-96515800	Enhancers	Osteobl	bone
45	chr8:96515600-96516000	Enhancers	Stomach Smooth Muscle	stomach
46	chr8:96515600-96516200	Enhancers	Fetal Stomach	stomach
47	chr8:96515600-96516400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:96515800-96516000	Enhancers	HUVEC	blood vessel
49	chr8:96515800-96516200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr8:96515800-96516200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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