Variant report

Variant	nsv891132
Chromosome Location	chr8:86505353-86553992
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	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
2	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
3	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
4	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
5	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
6	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
7	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
8	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
9	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
10	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
11	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
12	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
13	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
14	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
15	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
16	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
17	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
18	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
20	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
24	E2F4	chr8:86547943-86548263	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr8:86505700-86505895	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr8:86548212-86548420	GM12878	blood:	n/a	chr8:86548316-86548326
28	EP300	chr8:86530109-86530133	K562	blood:	n/a	n/a
29	FOS	chr8:86526689-86526696	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:86544593-86544999	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:86544590-86544994	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:86547861-86548371	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
33	FOS	chr8:86544555-86544966	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:86505653-86505944	MCF10A-Er-Src	breast:	n/a	chr8:86505807-86505815
35	FOS	chr8:86544592-86544996	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:86526559-86526927	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:86505726-86505871	MCF10A-Er-Src	breast:	n/a	chr8:86505807-86505815
38	FOS	chr8:86547443-86547509	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:86547900-86548453	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
40	FOS	chr8:86547867-86548278	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
41	FOS	chr8:86526691-86526802	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:86547885-86548430	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
43	FOSL1	chr8:86544544-86545033	HCT-116	colon:	n/a	n/a
44	FOSL1	chr8:86544543-86545175	HCT-116	colon:	n/a	n/a
45	FOSL2	chr8:86544559-86545076	MCF-7	breast:	n/a	n/a
46	FOXA2	chr8:86507937-86508266	A549	lung:	n/a	n/a
47	GATA2	chr8:86529877-86530241	K562	blood:	n/a	n/a
48	GATA3	chr8:86518345-86518505	SH-SY5Y	brain:	n/a	n/a
49	JUND	chr8:86505704-86505878	H1-hESC	embryonic stem cell:	n/a	chr8:86505807-86505815
50	MAFF	chr8:86513264-86513577	HepG2	liver:	n/a	chr8:86513383-86513401

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86551492-86551542	HMEC	breast:	n/a
2	chr8:86551492-86551542	CMK	blood:	n/a
3	chr8:86551492-86551542	U87	brain:	n/a
4	chr8:86551492-86551542	NT2-D1	testis:	n/a
5	chr8:86551492-86551542	SAEC	small airway:	n/a
6	chr8:86551492-86551542	HNPCEpiC	eye:	n/a
7	chr8:86551492-86551542	AG04449	skin:	fetal
8	chr8:86551492-86551542	HCM	heart:	n/a
9	chr8:86551492-86551542	GM06990	blood:	n/a
10	chr8:86551492-86551542	MCF10A-Er-Src	breast:	n/a
11	chr8:86551492-86551542	H1-hESC	embryonic stem cell:	embryo
12	chr8:86551492-86551542	HUVEC	blood vessel:	n/a
13	chr8:86551492-86551542	GM12891	blood:	n/a
14	chr8:86551492-86551542	GM12892	blood:	n/a
15	chr8:86551492-86551542	AoSMC	blood vessel:	n/a
16	chr8:86551492-86551542	NH-A	brain:	n/a
17	chr8:86551492-86551542	AG10803	skin:	n/a
18	chr8:86551492-86551542	PFSK-1	brain:	n/a
19	chr8:86551492-86551542	Hepatocyte	liver:	n/a
20	chr8:86551492-86551542	AG04450	lung:	fetal
21	chr8:86551492-86551542	NB4	blood:	n/a
22	chr8:86551492-86551542	SK-N-SH_RA	brain:	n/a
23	chr8:86551492-86551542	SK-N-SH	brain:	n/a
24	chr8:86551492-86551542	HIPEpiC	eye:	n/a
25	chr8:86551492-86551542	Jurkat	blood:	n/a
26	chr8:86551492-86551542	HepG2	liver:	n/a
27	chr8:86551492-86551542	HRE	kidney:	n/a
28	chr8:86551492-86551542	K562	blood:	n/a
29	chr8:86551492-86551542	NHBE	bronchial:	n/a
30	chr8:86551492-86551542	RPTEC	kidney:	n/a
31	chr8:86551492-86551542	HCF	heart:	n/a
32	chr8:86551492-86551542	HRPEpiC	eye:	n/a
33	chr8:86551492-86551542	A549	lung:	n/a
34	chr8:86551492-86551542	HEK293	kidney:	embryo
35	chr8:86551492-86551542	HCT-116	colon:	n/a
36	chr8:86551492-86551542	BE2_C	brain:	n/a
37	chr8:86551492-86551542	HRCEpiC	kidney:	n/a
38	chr8:86551492-86551542	GM12878	blood:	n/a
39	chr8:86551492-86551542	AG09309	skin:	n/a
40	chr8:86551492-86551542	Caco-2	colon:	n/a
41	chr8:86551492-86551542	ovcar-3	ovarian:	n/a
42	chr8:86551492-86551542	NHDF-neo	bronchial:	n/a
43	chr8:86551492-86551542	AG09319	gingival:	n/a
44	chr8:86551492-86551542	BJ	skin:	n/a
45	chr8:86551492-86551542	ProgFib	skin:	n/a
46	chr8:86551492-86551542	PANC-1	pancreas:	n/a
47	chr8:86551492-86551542	HL-60	blood:	n/a
48	chr8:86551492-86551542	Hela-S3	cervix:	n/a
49	chr8:86551492-86551542	HCPEpiC	choroid plexus:	n/a
50	chr8:86551492-86551542	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:
2	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
3	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
4	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
5	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
6	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:

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

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

Extended variants
information (count: 1078 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7817848	chr8:86505353-86505354	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75182026	chr8:86505358-86505359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558764808	chr8:86505374-86505375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78848742	chr8:86505385-86505386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191801651	chr8:86505405-86505406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554517368	chr8:86505448-86505449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140977354	chr8:86505465-86505466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540481699	chr8:86505518-86505519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553787568	chr8:86505588-86505589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150228094	chr8:86505591-86505592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115830815	chr8:86505657-86505658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145704487	chr8:86505671-86505672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540122895	chr8:86505757-86505758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375965607	chr8:86505772-86505773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531413032	chr8:86505788-86505789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541962279	chr8:86505824-86505825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561628058	chr8:86505874-86505875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181313148	chr8:86505982-86505983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72684803	chr8:86505996-86505997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186324515	chr8:86506039-86506040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567041358	chr8:86506050-86506051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532874092	chr8:86506052-86506053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534619559	chr8:86506206-86506207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552866355	chr8:86506237-86506238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189944877	chr8:86506291-86506292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34711440	chr8:86506333-86506334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569126946	chr8:86506338-86506339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374623102	chr8:86506368-86506369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368962086	chr8:86506395-86506396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112231273	chr8:86506396-86506397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182149652	chr8:86506398-86506399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568397942	chr8:86506435-86506436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374661083	chr8:86506458-86506459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533939420	chr8:86506480-86506481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554180312	chr8:86506486-86506487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577049530	chr8:86506513-86506514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546147520	chr8:86506523-86506524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7017985	chr8:86506567-86506568	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6992210	chr8:86506572-86506573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541899280	chr8:86506682-86506683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75965236	chr8:86506766-86506767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373881322	chr8:86506787-86506788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561624609	chr8:86506798-86506799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138211286	chr8:86506807-86506808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540652690	chr8:86506864-86506865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143594349	chr8:86506881-86506882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186725924	chr8:86506883-86506884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552470461	chr8:86506888-86506889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542318759	chr8:86506927-86506928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562704996	chr8:86506937-86506938	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:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86502200-86508600	Weak transcription	Thymus	Thymus
2	chr8:86502400-86506200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:86502400-86508400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:86502600-86505800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:86502600-86506400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr8:86503000-86508200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:86503200-86506800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:86504000-86506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:86504200-86505400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:86504200-86505400	Weak transcription	Brain Angular Gyrus	brain
11	chr8:86504200-86505400	Weak transcription	Stomach Mucosa	stomach
12	chr8:86504200-86506000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:86504200-86506200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:86504200-86506600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:86504200-86506800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:86504200-86508400	Weak transcription	Primary T cells from cord blood	blood
17	chr8:86504200-86509600	Weak transcription	Fetal Kidney	kidney
18	chr8:86504400-86505800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:86504400-86506200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr8:86504600-86505800	Weak transcription	Brain Substantia Nigra	brain
21	chr8:86504800-86505600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:86504800-86506000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr8:86504800-86506400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:86505200-86505400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr8:86505200-86505400	Enhancers	Brain Hippocampus Middle	brain
26	chr8:86505200-86505800	Enhancers	Brain Cingulate Gyrus	brain
27	chr8:86505200-86506400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:86505400-86505800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:86505400-86506000	Enhancers	Stomach Mucosa	stomach
30	chr8:86505400-86506400	Enhancers	Brain Angular Gyrus	brain
31	chr8:86505600-86506000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr8:86505800-86506200	Enhancers	Brain Substantia Nigra	brain
33	chr8:86505800-86508400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:86505800-86509400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:86505800-86509400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:86506000-86506200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr8:86506000-86508200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr8:86506000-86508400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr8:86506000-86508400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr8:86506000-86509000	Weak transcription	Stomach Mucosa	stomach
41	chr8:86506200-86508400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr8:86506200-86508400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr8:86506200-86508400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:86506200-86508400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr8:86506400-86506800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:86506400-86508200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr8:86506400-86508200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr8:86506600-86508400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:86506800-86507000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:86506800-86507000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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