Variant report

Variant	nsv968495
Chromosome Location	chr8:90835687-90842298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:104)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:104 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90838811-90838957	HepG2	liver:	n/a	n/a
2	BACH1	chr8:90835853-90835861	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:90838425-90838937	GM12878	blood:	n/a	n/a
4	BRCA1	chr8:90838179-90838327	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:90840754-90840941	A549	lung:	n/a	n/a
6	CEBPB	chr8:90840694-90841001	HepG2	liver:	n/a	n/a
7	CHD2	chr8:90838378-90838823	GM12878	blood:	n/a	n/a
8	CHD2	chr8:90836673-90836894	HepG2	liver:	n/a	n/a
9	CTCF	chr8:90837760-90837910	HCFaa	heart:	n/a	n/a
10	CTCF	chr8:90837720-90837870	GM12865	blood:	n/a	n/a
11	CTCF	chr8:90837760-90837910	HAc	cerebellar:	n/a	n/a
12	CTCF	chr8:90837720-90837870	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr8:90837840-90837990	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:90837740-90837890	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:90837700-90837850	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr8:90837660-90837810	BE2_C	brain:	n/a	n/a
17	CTCF	chr8:90837780-90837930	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr8:90837740-90837890	AG04450	lung:	n/a	n/a
19	CTCF	chr8:90837740-90837890	GM12874	blood:	n/a	n/a
20	CTCF	chr8:90837720-90837870	GM12872	blood:	n/a	n/a
21	CTCF	chr8:90837740-90837890	GM12873	blood:	n/a	n/a
22	CTCF	chr8:90837760-90837910	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr8:90837740-90837890	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr8:90837660-90837810	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr8:90837720-90837870	HMF	breast:	n/a	n/a
26	CTCF	chr8:90837700-90837850	GM12878	blood:	n/a	n/a
27	CTCF	chr8:90837900-90838050	A549	lung:	n/a	n/a
28	CTCF	chr8:90837700-90837850	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr8:90837760-90837910	GM06990	blood:	n/a	n/a
30	CTCF	chr8:90837800-90837950	GM12875	blood:	n/a	n/a
31	CTCF	chr8:90837780-90837930	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr8:90837770-90837953	K562	blood:	n/a	n/a
33	CTCF	chr8:90837740-90837890	HepG2	liver:	n/a	n/a
34	CTCF	chr8:90837780-90837930	HMF	breast:	n/a	n/a
35	EBF1	chr8:90841497-90841595	GM12878	blood:	n/a	chr8:90841531-90841542
36	EBF1	chr8:90838506-90838940	GM12878	blood:	n/a	chr8:90838835-90838846
37	ELK1	chr8:90838284-90838367	GM12878	blood:	n/a	n/a
38	EP300	chr8:90838176-90838632	GM12878	blood:	n/a	chr8:90838472-90838481 chr8:90838468-90838482
39	EP300	chr8:90838518-90838653	GM12878	blood:	n/a	n/a
40	FOXA1	chr8:90838495-90838856	HepG2	liver:	n/a	n/a
41	FOXA2	chr8:90838518-90838932	A549	lung:	n/a	n/a
42	FOXA2	chr8:90838663-90838912	HepG2	liver:	n/a	n/a
43	FOXA2	chr8:90838522-90839106	A549	lung:	n/a	n/a
44	GATA3	chr8:90840327-90840383	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr8:90838161-90839200	SK-N-SH	brain:	n/a	chr8:90838470-90838480
46	GTF2F1	chr8:90836908-90836944	H1-hESC	embryonic stem cell:	n/a	n/a
47	HNF4A	chr8:90836809-90837139	HepG2	liver:	n/a	chr8:90836928-90836943
48	IRF1	chr8:90837267-90837276	K562	blood:	n/a	n/a
49	IRF3	chr8:90838899-90838902	GM12878	blood:	n/a	n/a
50	JUND	chr8:90838406-90838792	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90837663-90837713	NB4	blood:	n/a
2	chr8:90837663-90837713	HEK293	kidney:	embryo
3	chr8:90837663-90837713	GM19239	blood:	n/a
4	chr8:90837663-90837713	SK-N-SH_RA	brain:	n/a
5	chr8:90837663-90837713	Jurkat	blood:	n/a
6	chr8:90837663-90837713	AG04450	lung:	fetal
7	chr8:90837663-90837713	HL-60	blood:	n/a
8	chr8:90837663-90837713	GM12891	blood:	n/a
9	chr8:90837663-90837713	RPTEC	kidney:	n/a
10	chr8:90837663-90837713	HRPEpiC	eye:	n/a
11	chr8:90837663-90837713	PFSK-1	brain:	n/a
12	chr8:90837663-90837713	GM12892	blood:	n/a
13	chr8:90837663-90837713	SK-N-SH	brain:	n/a
14	chr8:90837663-90837713	HUVEC	blood vessel:	n/a
15	chr8:90837663-90837713	NT2-D1	testis:	n/a
16	chr8:90837663-90837713	HCPEpiC	choroid plexus:	n/a
17	chr8:90837663-90837713	ovcar-3	ovarian:	n/a
18	chr8:90837663-90837713	BJ	skin:	n/a
19	chr8:90837663-90837713	Hela-S3	cervix:	n/a
20	chr8:90837663-90837713	AG10803	skin:	n/a
21	chr8:90837663-90837713	K562	blood:	n/a
22	chr8:90837663-90837713	MCF-7	breast:	n/a
23	chr8:90837663-90837713	U87	brain:	n/a
24	chr8:90837663-90837713	AG04449	skin:	fetal
25	chr8:90837663-90837713	T-47D	breast:	n/a
26	chr8:90837663-90837713	HCT-116	colon:	n/a
27	chr8:90837663-90837713	BE2_C	brain:	n/a
28	chr8:90837663-90837713	SAEC	small airway:	n/a
29	chr8:90837663-90837713	AoSMC	blood vessel:	n/a
30	chr8:90837663-90837713	HAEpiC	amniotic membrane:	n/a
31	chr8:90837663-90837713	LNCaP	prostate:	n/a
32	chr8:90837663-90837713	Hepatocyte	liver:	n/a
33	chr8:90837663-90837713	HIPEpiC	eye:	n/a
34	chr8:90837663-90837713	Caco-2	colon:	n/a
35	chr8:90837663-90837713	NHDF-neo	bronchial:	n/a
36	chr8:90837663-90837713	AG09309	skin:	n/a
37	chr8:90837663-90837713	IMR90	lung:	fetal
38	chr8:90837663-90837713	PANC-1	pancreas:	n/a
39	chr8:90837663-90837713	HEEpiC	esophagus:	n/a
40	chr8:90837663-90837713	HCF	heart:	n/a
41	chr8:90837663-90837713	ECC-1	luminal epithelium:	n/a
42	chr8:90837663-90837713	HRE	kidney:	n/a
43	chr8:90837663-90837713	HCM	heart:	n/a
44	chr8:90837663-90837713	NHBE	bronchial:	n/a
45	chr8:90837663-90837713	PrEC	prostate:	n/a
46	chr8:90837663-90837713	HMEC	breast:	n/a
47	chr8:90837663-90837713	GM06990	blood:	n/a
48	chr8:90837663-90837713	HepG2	liver:	n/a
49	chr8:90837663-90837713	NH-A	brain:	n/a
50	chr8:90837663-90837713	SK-N-MC	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90838136..90841638-chr8:90842560..90845111,3	K562	blood:
2	chr8:90836699..90839189-chr8:90853198..90855476,2	MCF-7	breast:
3	chr8:90838601..90840941-chr8:90843850..90846321,2	MCF-7	breast:
4	chr8:90841090..90842981-chr8:90920708..90922317,2	MCF-7	breast:
5	chr8:90838578..90843611-chr8:90912392..90915640,4	MCF-7	breast:
6	chr8:90841193..90842876-chr8:90844123..90846004,2	MCF-7	breast:
7	chr8:90835014..90836804-chr8:90836875..90838600,2	K562	blood:
8	chr8:90842015..90844808-chr8:90846350..90848041,2	MCF-7	breast:
9	chr8:90835853..90837817-chr8:90838818..90840749,2	MCF-7	breast:
10	chr8:90800222..90801982-chr8:90840675..90842723,2	MCF-7	breast:
11	chr8:90824515..90827081-chr8:90836313..90840458,3	MCF-7	breast:
12	chr8:90783067..90785641-chr8:90833540..90835924,2	MCF-7	breast:
13	chr8:90835454..90837187-chr8:90837338..90840296,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-4	chr8:90835776-90836030	NONHSAT127628
2	lnc-NBN-5	chr8:90838399-90839074	ucscGeneNc_uc003yed_1

No data

Variant related genes	Relation type
COX6B1P6	TF binding region
COX6B1P6	CpG island
ENSG00000253349	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000164823	chromatin interactions

Extended variants
information (count: 247 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:247 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180962275	chr8:90835708-90835709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369058134	chr8:90835742-90835743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561746994	chr8:90835743-90835744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373256681	chr8:90835763-90835764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376518874	chr8:90835841-90835842	Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
6	rs369604613	chr8:90835878-90835879	Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
7	rs148772010	chr8:90835902-90835903	Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
8	rs548758080	chr8:90835927-90835928	Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
9	rs43135	chr8:90835950-90835951	Weak transcription Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs534516667	chr8:90836003-90836004	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs453266	chr8:90836017-90836018	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs559308185	chr8:90836065-90836066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576878945	chr8:90836090-90836091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142197425	chr8:90836092-90836093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374584079	chr8:90836098-90836099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369771	chr8:90836112-90836113	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs370240783	chr8:90836121-90836122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184321585	chr8:90836132-90836133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541589335	chr8:90836144-90836145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563484274	chr8:90836152-90836153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575113253	chr8:90836153-90836154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146391404	chr8:90836190-90836191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564045144	chr8:90836205-90836206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs39770	chr8:90836233-90836234	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs547763350	chr8:90836268-90836269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554008093	chr8:90836272-90836273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530185734	chr8:90836298-90836299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72440016	chr8:90836310-90836311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368882163	chr8:90836311-90836312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371755072	chr8:90836312-90836313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374887869	chr8:90836313-90836314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139778997	chr8:90836339-90836340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189600755	chr8:90836377-90836378	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs535381060	chr8:90836385-90836386	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs181089647	chr8:90836397-90836398	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567998460	chr8:90836443-90836444	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372234010	chr8:90836469-90836470	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs117770316	chr8:90836471-90836472	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs185679332	chr8:90836496-90836497	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375597183	chr8:90836510-90836511	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372636951	chr8:90836516-90836517	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs73298609	chr8:90836540-90836541	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572801575	chr8:90836553-90836554	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs73694502	chr8:90836561-90836562	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs571682914	chr8:90836582-90836583	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs454561	chr8:90836615-90836616	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs113385376	chr8:90836626-90836627	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs369007443	chr8:90836645-90836646	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs563774314	chr8:90836660-90836661	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531085561	chr8:90836669-90836670	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90824000-90836600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:90828000-90845800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:90835800-90836000	Bivalent Enhancer	HepG2	liver
4	chr8:90836000-90836600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr8:90836400-90836600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr8:90836400-90836600	Active TSS	HepG2	liver
7	chr8:90836400-90837000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:90836400-90837000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:90836400-90837200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:90836400-90837200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:90836400-90837200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr8:90836400-90837800	Enhancers	Fetal Intestine Large	intestine
13	chr8:90836600-90837000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr8:90836600-90837000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:90836600-90837000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:90836600-90837000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:90836600-90837000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr8:90836600-90837000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:90836600-90837000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:90836600-90837200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr8:90836600-90837200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:90836600-90837200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:90836600-90837200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr8:90836600-90837200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:90836600-90837200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr8:90836600-90837200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:90836600-90837400	Enhancers	Fetal Intestine Small	intestine
28	chr8:90836600-90837400	Flanking Active TSS	HepG2	liver
29	chr8:90836600-90837600	Enhancers	Stomach Mucosa	stomach
30	chr8:90836800-90837200	ZNF genes & repeats	Pancreas	Pancrea
31	chr8:90836800-90837600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:90836800-90838200	Enhancers	A549	lung
33	chr8:90836800-90838400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:90836800-90839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:90837000-90837400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:90837000-90837800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:90837000-90838200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr8:90837000-90838200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:90837000-90838200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr8:90837000-90839000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:90837000-90847600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr8:90837200-90838200	Weak transcription	Pancreas	Pancrea
43	chr8:90837200-90838400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr8:90837200-90844600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr8:90837400-90837800	Enhancers	HepG2	liver
46	chr8:90837400-90838200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr8:90837400-90838400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:90837600-90838000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr8:90837600-90838000	Weak transcription	Stomach Mucosa	stomach
50	chr8:90837600-90839200	Enhancers	Muscle Satellite Cultured Cells	--

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