Variant report

Variant	esv3399995
Chromosome Location	chr8:89672885-89710176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:89673622-89673674	K562	blood:	n/a	n/a
2	BRCA1	chr8:89685120-89685458	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr8:89687214-89687449	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:89684794-89685486	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:89709010-89709387	Hela-S3	cervix:	n/a	chr8:89709182-89709195
6	CEBPZ	chr8:89673802-89673880	HepG2	liver:	n/a	n/a
7	CHD2	chr8:89684892-89685406	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr8:89697780-89697930	HCFaa	heart:	n/a	n/a
9	CTCF	chr8:89697780-89697930	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr8:89684397-89684470	GM10248	blood:	n/a	n/a
11	CTCF	chr8:89697800-89697950	HEK293	kidney:	n/a	n/a
12	CTCF	chr8:89697800-89697950	MCF-7	breast:	n/a	n/a
13	CTCF	chr8:89697706-89697794	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:89697820-89697970	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:89684460-89684525	LNCaP	prostate:	n/a	n/a
16	CTCF	chr8:89697800-89697950	HMF	breast:	n/a	n/a
17	CTCF	chr8:89697720-89697870	A549	lung:	n/a	n/a
18	CTCF	chr8:89697720-89697810	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:89698359-89698676	K562	blood:	n/a	n/a
20	CTCF	chr8:89697760-89697910	HMEC	breast:	n/a	n/a
21	CTCF	chr8:89697712-89697827	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:89695869-89695895	Lung_OC	lung:	n/a	n/a
23	CTCF	chr8:89679604-89679645	GM13976	blood:	n/a	n/a
24	CTCF	chr8:89697740-89697890	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:89697760-89697910	GM12866	blood:	n/a	n/a
26	CTCF	chr8:89697720-89697870	HepG2	liver:	n/a	n/a
27	CTCF	chr8:89684675-89684721	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:89697740-89697890	HCT-116	colon:	n/a	n/a
29	CTCF	chr8:89690600-89690750	MCF-7	breast:	n/a	n/a
30	EP300	chr8:89684878-89685491	Hela-S3	cervix:	n/a	n/a
31	EP300	chr8:89709054-89709364	Hela-S3	cervix:	n/a	chr8:89709329-89709343
32	EP300	chr8:89680866-89681151	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr8:89680900-89681156	SK-N-SH_RA	brain:	n/a	n/a
34	FOS	chr8:89709000-89709393	MCF10A-Er-Src	breast:	n/a	chr8:89709200-89709208 chr8:89709200-89709207
35	FOS	chr8:89709059-89709432	HUVEC	blood vessel:	n/a	chr8:89709200-89709208 chr8:89709200-89709207
36	FOS	chr8:89684804-89685336	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:89709030-89709385	MCF10A-Er-Src	breast:	n/a	chr8:89709200-89709208 chr8:89709200-89709207
38	FOS	chr8:89684843-89685172	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:89684804-89685364	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:89684802-89685336	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:89709035-89709566	MCF10A-Er-Src	breast:	n/a	chr8:89709200-89709208 chr8:89709200-89709207
42	FOS	chr8:89709036-89709349	MCF10A-Er-Src	breast:	n/a	chr8:89709200-89709208 chr8:89709200-89709207
43	FOXA1	chr8:89698262-89698448	HepG2	liver:	n/a	n/a
44	FOXA1	chr8:89697715-89697992	T-47D	breast:	n/a	n/a
45	FOXA1	chr8:89698264-89698409	T-47D	breast:	n/a	n/a
46	FOXA2	chr8:89698051-89698600	A549	lung:	n/a	n/a
47	FOXA2	chr8:89676531-89676754	A549	lung:	n/a	n/a
48	FOXA2	chr8:89698275-89698517	A549	lung:	n/a	n/a
49	GATA2	chr8:89680905-89681368	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr8:89680900-89681344	SH-SY5Y	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89688501-89688551	SK-N-SH	brain:	n/a
2	chr8:89687477-89687527	SK-N-MC	brain:	n/a
3	chr8:89688361-89688411	Jurkat	blood:	n/a
4	chr8:89688501-89688551	HepG2	liver:	n/a
5	chr8:89688361-89688411	H1-hESC	embryonic stem cell:	embryo
6	chr8:89688501-89688551	PrEC	prostate:	n/a
7	chr8:89688501-89688551	Caco-2	colon:	n/a
8	chr8:89688501-89688551	HAEpiC	amniotic membrane:	n/a
9	chr8:89688361-89688411	AG09319	gingival:	n/a
10	chr8:89687477-89687527	HEEpiC	esophagus:	n/a
11	chr8:89688501-89688551	NHBE	bronchial:	n/a
12	chr8:89687477-89687527	HMEC	breast:	n/a
13	chr8:89687477-89687527	GM12878	blood:	n/a
14	chr8:89688361-89688411	HRE	kidney:	n/a
15	chr8:89688501-89688551	MCF-7	breast:	n/a
16	chr8:89687477-89687527	ProgFib	skin:	n/a
17	chr8:89688501-89688551	HCT-116	colon:	n/a
18	chr8:89688361-89688411	T-47D	breast:	n/a
19	chr8:89688501-89688551	AG04449	skin:	fetal
20	chr8:89687477-89687527	Hepatocyte	liver:	n/a
21	chr8:89688361-89688411	AG09309	skin:	n/a
22	chr8:89687477-89687527	ovcar-3	ovarian:	n/a
23	chr8:89688501-89688551	ECC-1	luminal epithelium:	n/a
24	chr8:89687477-89687527	SK-N-SH	brain:	n/a
25	chr8:89688501-89688551	T-47D	breast:	n/a
26	chr8:89688501-89688551	BE2_C	brain:	n/a
27	chr8:89687477-89687527	HL-60	blood:	n/a
28	chr8:89688361-89688411	PrEC	prostate:	n/a
29	chr8:89688361-89688411	GM19239	blood:	n/a
30	chr8:89688501-89688551	GM19239	blood:	n/a
31	chr8:89688501-89688551	A549	lung:	n/a
32	chr8:89688361-89688411	CMK	blood:	n/a
33	chr8:89687477-89687527	HRE	kidney:	n/a
34	chr8:89687477-89687527	GM12891	blood:	n/a
35	chr8:89688361-89688411	HRCEpiC	kidney:	n/a
36	chr8:89687477-89687527	K562	blood:	n/a
37	chr8:89688361-89688411	SK-N-SH	brain:	n/a
38	chr8:89687477-89687527	PrEC	prostate:	n/a
39	chr8:89688361-89688411	GM12891	blood:	n/a
40	chr8:89688361-89688411	GM12892	blood:	n/a
41	chr8:89687477-89687527	SKMC	muscle:	n/a
42	chr8:89687477-89687527	T-47D	breast:	n/a
43	chr8:89688361-89688411	HRPEpiC	eye:	n/a
44	chr8:89688501-89688551	AG09319	gingival:	n/a
45	chr8:89688501-89688551	PFSK-1	brain:	n/a
46	chr8:89688501-89688551	NB4	blood:	n/a
47	chr8:89687477-89687527	CMK	blood:	n/a
48	chr8:89688501-89688551	HUVEC	blood vessel:	n/a
49	chr8:89688501-89688551	GM12891	blood:	n/a
50	chr8:89688361-89688411	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:89663321..89665124-chr8:89674898..89677154,2	MCF-7	breast:
2	chr8:89690069..89691649-chr8:89726011..89728542,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP16-3	chr8:89680110-89680241	l_3638_chr8:89634036-89669812_testes

No data

Variant related genes	Relation type
ENSG00000253553	TF binding region
ENSG00000253553	CpG island

Extended variants
information (count: 513 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:513 , 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	rs140613189	chr8:89680113-89680114	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs541343250	chr8:89680162-89680163	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs555422192	chr8:89682818-89682819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573910612	chr8:89682844-89682845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544370793	chr8:89682846-89682847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557156500	chr8:89682851-89682852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34542316	chr8:89682873-89682874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562844131	chr8:89682875-89682876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372859428	chr8:89682906-89682907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151244070	chr8:89682917-89682918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545673495	chr8:89682926-89682927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569077527	chr8:89682934-89682935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140408707	chr8:89682936-89682937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539754948	chr8:89682947-89682948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192313782	chr8:89682951-89682952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561332655	chr8:89682952-89682953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371781237	chr8:89683018-89683019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376201847	chr8:89683070-89683071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184873456	chr8:89683139-89683140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550750189	chr8:89683195-89683196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545139797	chr8:89684442-89684443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201933317	chr8:89684448-89684449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191863415	chr8:89684508-89684509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200557938	chr8:89684513-89684514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201272885	chr8:89684531-89684532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377203981	chr8:89684635-89684636	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs548862122	chr8:89684636-89684637	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs7820908	chr8:89684637-89684638	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs531193415	chr8:89684658-89684659	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs549481264	chr8:89684692-89684693	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7833089	chr8:89684726-89684727	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538862398	chr8:89684733-89684734	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs554303352	chr8:89684753-89684754	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs527333541	chr8:89684765-89684766	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527877055	chr8:89684788-89684789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs34652332	chr8:89684789-89684790	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs147986586	chr8:89684804-89684805	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs371376628	chr8:89684805-89684806	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs555281892	chr8:89684814-89684815	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs569700455	chr8:89684881-89684882	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs576518319	chr8:89684886-89684887	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs537411097	chr8:89684915-89684916	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs181911428	chr8:89684970-89684971	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs577225076	chr8:89685062-89685063	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560521492	chr8:89685098-89685099	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs11991077	chr8:89685138-89685139	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs560340832	chr8:89685140-89685141	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs572125804	chr8:89685147-89685148	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs542548848	chr8:89685165-89685166	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs560815497	chr8:89685190-89685191	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89682800-89683200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:89684400-89684600	Enhancers	Hela-S3	cervix
3	chr8:89684600-89684800	Flanking Active TSS	Hela-S3	cervix
4	chr8:89684600-89685400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:89684800-89685200	Active TSS	Hela-S3	cervix
6	chr8:89685200-89685400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:89685200-89685600	Flanking Active TSS	Hela-S3	cervix
8	chr8:89685400-89687400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:89685400-89690600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr8:89685600-89686000	Enhancers	Hela-S3	cervix
11	chr8:89687000-89687200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:89687200-89688000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr8:89687400-89688800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:89688000-89688800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr8:89688000-89688800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:89688200-89689000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:89688800-89690200	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr8:89688800-89690600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:89690200-89691000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:89690600-89690800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:89690600-89691000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:89690600-89691400	Enhancers	Fetal Heart	heart
23	chr8:89690600-89691400	Enhancers	Fetal Lung	lung
24	chr8:89693200-89693400	Enhancers	Fetal Lung	lung
25	chr8:89693200-89693600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:89693200-89693800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:89693200-89694200	Enhancers	Adipose Nuclei	Adipose
28	chr8:89693400-89693800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:89693600-89693800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:89693800-89694200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:89697800-89698000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr8:89697800-89698400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr8:89708000-89708600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:89708400-89709600	Enhancers	NH-A	brain
35	chr8:89708400-89709800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:89708400-89709800	Enhancers	Adipose Nuclei	Adipose
37	chr8:89708600-89709000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:89708600-89710000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:89708600-89710200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:89708600-89710200	Enhancers	HUVEC	blood vessel
41	chr8:89709000-89709800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:89709800-89710000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links