Variant report

Variant	nsv1032291
Chromosome Location	chr8:86476036-86557401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:612)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
2	BACH1	chr8:86477700-86478018	K562	blood:	n/a	n/a
3	BACH1	chr8:86477707-86478028	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:86557171-86557645	GM12878	blood:	n/a	n/a
5	BATF	chr8:86556713-86557155	GM12878	blood:	n/a	n/a
6	BATF	chr8:86556634-86557157	GM12878	blood:	n/a	n/a
7	BATF	chr8:86557168-86557577	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:86556317-86556493	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:86556627-86557168	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:86557171-86557821	GM12878	blood:	n/a	chr8:86557185-86557194
11	BCL11A	chr8:86556646-86557544	GM12878	blood:	n/a	chr8:86557185-86557194 chr8:86557162-86557171
12	BHLHE40	chr8:86557188-86557731	HepG2	liver:	n/a	n/a
13	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
14	BHLHE40	chr8:86556653-86557165	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
16	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
17	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
18	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
19	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
20	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
21	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
22	CEBPB	chr8:86483060-86483308	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
24	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
25	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
26	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
27	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
28	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
29	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
30	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
31	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
32	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr8:86482894-86483257	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:86488840-86488915	GM19240	blood:	n/a	n/a
35	CTCF	chr8:86501940-86502090	HRE	kidney:	n/a	n/a
36	CTCF	chr8:86488826-86488917	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:86488811-86488916	A549	lung:	n/a	n/a
38	CTCF	chr8:86500740-86500890	HCT-116	colon:	n/a	n/a
39	CTCF	chr8:86488877-86488897	GM19238	blood:	n/a	n/a
40	CTCF	chr8:86488799-86488917	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:86488793-86488916	ProgFib	skin:	n/a	n/a
42	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr8:86488825-86488916	GM12891	blood:	n/a	n/a
44	CTCF	chr8:86488806-86488916	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr8:86480580-86480730	HRE	kidney:	n/a	n/a
48	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr8:86494374-86494479	GM19239	blood:	n/a	n/a
50	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86551492-86551542	HRPEpiC	eye:	n/a
2	chr8:86486097-86486147	CMK	blood:	n/a
3	chr8:86551492-86551542	HRPEpiC	eye:	n/a
4	chr8:86486097-86486147	CMK	blood:	n/a
5	chr8:86556164-86556214	HEK293	kidney:	embryo
6	chr8:86504072-86504122	AG09319	gingival:	n/a
7	chr8:86554888-86554938	PANC-1	pancreas:	n/a
8	chr8:86554888-86554938	HMEC	breast:	n/a
9	chr8:86556164-86556214	NHDF-neo	bronchial:	n/a
10	chr8:86551492-86551542	GM19239	blood:	n/a
11	chr8:86556903-86556953	ECC-1	luminal epithelium:	n/a
12	chr8:86504072-86504122	T-47D	breast:	n/a
13	chr8:86556176-86556226	AG04449	skin:	fetal
14	chr8:86556171-86556221	NH-A	brain:	n/a
15	chr8:86554888-86554938	NH-A	brain:	n/a
16	chr8:86556164-86556214	SAEC	small airway:	n/a
17	chr8:86551492-86551542	ovcar-3	ovarian:	n/a
18	chr8:86554888-86554938	HRCEpiC	kidney:	n/a
19	chr8:86486097-86486147	AoSMC	blood vessel:	n/a
20	chr8:86554888-86554938	RPTEC	kidney:	n/a
21	chr8:86504072-86504122	HRE	kidney:	n/a
22	chr8:86556903-86556953	Jurkat	blood:	n/a
23	chr8:86504072-86504122	GM12892	blood:	n/a
24	chr8:86556176-86556226	BE2_C	brain:	n/a
25	chr8:86556176-86556226	AG09319	gingival:	n/a
26	chr8:86504072-86504122	Jurkat	blood:	n/a
27	chr8:86554026-86554076	AG09309	skin:	n/a
28	chr8:86504072-86504122	HCF	heart:	n/a
29	chr8:86556176-86556226	BJ	skin:	n/a
30	chr8:86504072-86504122	SK-N-MC	brain:	n/a
31	chr8:86554888-86554938	GM12892	blood:	n/a
32	chr8:86556176-86556226	HCT-116	colon:	n/a
33	chr8:86554888-86554938	IMR90	lung:	fetal
34	chr8:86504072-86504122	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:86556749-86556799	Hepatocyte	liver:	n/a
36	chr8:86556903-86556953	PANC-1	pancreas:	n/a
37	chr8:86504072-86504122	GM12891	blood:	n/a
38	chr8:86554026-86554076	RPTEC	kidney:	n/a
39	chr8:86554888-86554938	NHBE	bronchial:	n/a
40	chr8:86556171-86556221	AG04449	skin:	fetal
41	chr8:86556749-86556799	HCF	heart:	n/a
42	chr8:86556164-86556214	ECC-1	luminal epithelium:	n/a
43	chr8:86551492-86551542	HUVEC	blood vessel:	n/a
44	chr8:86556164-86556214	Hepatocyte	liver:	n/a
45	chr8:86556749-86556799	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:86551492-86551542	AG10803	skin:	n/a
47	chr8:86486097-86486147	SAEC	small airway:	n/a
48	chr8:86554888-86554938	HRPEpiC	eye:	n/a
49	chr8:86556176-86556226	AoSMC	blood vessel:	n/a
50	chr8:86556164-86556214	HMEC	breast:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86375239..86377397-chr8:86481535..86484020,2	MCF-7	breast:
2	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
3	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
4	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
5	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
6	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
7	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
8	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
9	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
10	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
11	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
12	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:
13	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
14	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537
2	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
REXO1L8P	TF binding region
ENSG00000253680	CpG island
REXO1L8P	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 2200 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576740214	chr8:86476039-86476040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371788463	chr8:86476102-86476103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117790823	chr8:86476124-86476125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568324488	chr8:86476130-86476131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113127736	chr8:86476199-86476200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187314676	chr8:86476203-86476204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536038238	chr8:86476205-86476206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376785277	chr8:86476206-86476207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531229058	chr8:86476235-86476236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79315064	chr8:86476247-86476248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77544501	chr8:86476302-86476303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372423894	chr8:86476384-86476385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530345861	chr8:86476404-86476405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79995540	chr8:86476417-86476418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566865623	chr8:86476429-86476430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566696745	chr8:86476433-86476434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191800455	chr8:86476439-86476440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552289794	chr8:86476440-86476441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568955527	chr8:86476450-86476451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1017427	chr8:86476469-86476470	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182518950	chr8:86476504-86476505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567888577	chr8:86476546-86476547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113592708	chr8:86476549-86476550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370377106	chr8:86476569-86476570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553790826	chr8:86476585-86476586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370595591	chr8:86476586-86476587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372902372	chr8:86476587-86476588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200630712	chr8:86476589-86476590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201601759	chr8:86476591-86476592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376088264	chr8:86476605-86476606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2934016	chr8:86476608-86476609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187746809	chr8:86476609-86476610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555910124	chr8:86476613-86476614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529119149	chr8:86476617-86476618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544395383	chr8:86476621-86476622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370427178	chr8:86476629-86476630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10111569	chr8:86476630-86476631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368681365	chr8:86476633-86476634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144171352	chr8:86476634-86476635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs58785417	chr8:86476647-86476648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56701774	chr8:86476649-86476650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs56239378	chr8:86476667-86476668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199916882	chr8:86476673-86476674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373846207	chr8:86476681-86476682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192549785	chr8:86476684-86476685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185562769	chr8:86476685-86476686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190519475	chr8:86476688-86476689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148846751	chr8:86476735-86476736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556186394	chr8:86476740-86476741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570535074	chr8:86476743-86476744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Autism	22495311	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
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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Acute lymphoblastic leukemia	18458336	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 monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86474600-86476600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:86475400-86476200	Enhancers	Brain Hippocampus Middle	brain
3	chr8:86475400-86480600	Weak transcription	Fetal Intestine Small	intestine
4	chr8:86475400-86480800	Weak transcription	Fetal Intestine Large	intestine
5	chr8:86475400-86481000	Weak transcription	Brain Anterior Caudate	brain
6	chr8:86476000-86477200	Enhancers	HMEC	breast
7	chr8:86476000-86480600	Weak transcription	Brain Substantia Nigra	brain
8	chr8:86476200-86480600	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:86476600-86481200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:86476800-86477600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:86477000-86477400	Enhancers	Esophagus	oesophagus
12	chr8:86477200-86482600	Weak transcription	HMEC	breast
13	chr8:86479000-86482400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:86480400-86480800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr8:86480400-86481200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr8:86480400-86481600	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:86480600-86481000	Enhancers	Brain Substantia Nigra	brain
18	chr8:86480600-86481600	Enhancers	Brain Angular Gyrus	brain
19	chr8:86480600-86482200	Enhancers	Brain Hippocampus Middle	brain
20	chr8:86480600-86482200	Enhancers	Fetal Intestine Small	intestine
21	chr8:86480800-86481600	Enhancers	Fetal Lung	lung
22	chr8:86480800-86482200	Enhancers	Fetal Intestine Large	intestine
23	chr8:86480800-86487000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr8:86481000-86481200	Enhancers	Brain Anterior Caudate	brain
25	chr8:86481000-86481400	Flanking Active TSS	Brain Substantia Nigra	brain
26	chr8:86481000-86482200	Enhancers	Liver	Liver
27	chr8:86481200-86481600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr8:86481200-86481600	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr8:86481400-86481600	Active TSS	Brain Substantia Nigra	brain
30	chr8:86481600-86482200	Enhancers	Brain Substantia Nigra	brain
31	chr8:86481600-86485200	Weak transcription	Brain Anterior Caudate	brain
32	chr8:86481600-86486600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr8:86481600-86486800	Weak transcription	Brain Angular Gyrus	brain
34	chr8:86482200-86484800	Weak transcription	Brain Hippocampus Middle	brain
35	chr8:86482200-86485000	Weak transcription	Brain Substantia Nigra	brain
36	chr8:86482400-86484400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:86482400-86485000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:86482600-86483800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:86482600-86483800	Enhancers	HMEC	breast
40	chr8:86482600-86483800	Enhancers	NHEK	skin
41	chr8:86482800-86483200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:86483000-86483200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr8:86483200-86483400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr8:86483200-86486200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr8:86483400-86484800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:86483600-86483800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr8:86483800-86486200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr8:86484800-86485400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr8:86484800-86485400	Enhancers	Brain Hippocampus Middle	brain
50	chr8:86485000-86485400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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