Variant report

Variant	nsv609883
Chromosome Location	chr8:4610345-4777295
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	ARID3A	chr8:4691580-4691808	HepG2	liver:	n/a	n/a
2	BACH1	chr8:4703337-4703643	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:4754116-4754124	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:4691724-4691748	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:4772393-4772593	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:4775790-4776090	IMR90	lung:	n/a	chr8:4775928-4775939 chr8:4775926-4775937
7	CEBPB	chr8:4775823-4775999	H1-hESC	embryonic stem cell:	n/a	chr8:4775928-4775939 chr8:4775926-4775937
8	CEBPB	chr8:4772340-4772637	A549	lung:	n/a	n/a
9	CEBPB	chr8:4732872-4733196	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:4722926-4723126	HepG2	liver:	n/a	chr8:4723026-4723037
11	CEBPB	chr8:4775751-4776093	HepG2	liver:	n/a	chr8:4775928-4775939 chr8:4775926-4775937
12	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
13	CEBPB	chr8:4613708-4613813	A549	lung:	n/a	n/a
14	CEBPB	chr8:4775784-4776088	A549	lung:	n/a	chr8:4775928-4775939 chr8:4775926-4775937
15	CEBPB	chr8:4740653-4740819	HepG2	liver:	n/a	n/a
16	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
18	CTCF	chr8:4644551-4644864	K562	blood:	n/a	n/a
19	CTCF	chr8:4691468-4691633	MCF-7	breast:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
20	CTCF	chr8:4691384-4691641	SK-N-SH_RA	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
21	CTCF	chr8:4695440-4695590	HA-sp	spinal cord:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
22	CTCF	chr8:4695460-4695610	GM12878	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
23	CTCF	chr8:4695440-4695590	GM12873	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
24	CTCF	chr8:4733028-4733083	Spleen_OC	spleen:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
25	CTCF	chr8:4732980-4733130	NHEK	skin:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
26	CTCF	chr8:4732960-4733110	HCM	heart:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
27	CTCF	chr8:4695440-4695590	GM12864	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
28	CTCF	chr8:4691480-4691630	GM12801	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
29	CTCF	chr8:4691480-4691630	SK-N-SH_RA	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
30	CTCF	chr8:4732935-4733159	HepG2	liver:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
31	CTCF	chr8:4691420-4691570	GM06990	blood:	n/a	n/a
32	CTCF	chr8:4691500-4691650	GM12872	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
33	CTCF	chr8:4644597-4644867	HepG2	liver:	n/a	n/a
34	CTCF	chr8:4695406-4695628	MCF-7	breast:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
35	CTCF	chr8:4695460-4695610	NHEK	skin:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
36	CTCF	chr8:4732999-4733133	Fibrobl	skin:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
37	CTCF	chr8:4732991-4733133	GM12892	blood:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
38	CTCF	chr8:4695400-4695550	GM12872	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
39	CTCF	chr8:4691351-4691757	GM12878	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
40	CTCF	chr8:4691520-4691670	AG09319	gingival:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
41	CTCF	chr8:4644700-4644850	GM12875	blood:	n/a	n/a
42	CTCF	chr8:4732980-4733130	GM12865	blood:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
43	CTCF	chr8:4644640-4644790	GM12868	blood:	n/a	n/a
44	CTCF	chr8:4732951-4733197	SK-N-SH_RA	brain:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
45	CTCF	chr8:4733020-4733170	NB4	blood:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
46	CTCF	chr8:4695400-4695625	GM19240	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
47	CTCF	chr8:4695440-4695590	GM12868	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
48	CTCF	chr8:4690820-4690970	GM12872	blood:	n/a	n/a
49	CTCF	chr8:4733040-4733190	HAc	cerebellar:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066
50	CTCF	chr8:4732980-4733130	GM12878	blood:	n/a	chr8:4733043-4733064 chr8:4733049-4733065 chr8:4733048-4733066

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4773213-4773263	HCM	heart:	n/a
2	chr8:4750513-4750563	GM12891	blood:	n/a
3	chr8:4617087-4617137	HNPCEpiC	eye:	n/a
4	chr8:4750513-4750563	GM12878	blood:	n/a
5	chr8:4637584-4637634	HAEpiC	amniotic membrane:	n/a
6	chr8:4637584-4637634	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:4629524-4629574	HAEpiC	amniotic membrane:	n/a
8	chr8:4637584-4637634	SKMC	muscle:	n/a
9	chr8:4629524-4629574	Hela-S3	cervix:	n/a
10	chr8:4773213-4773263	HIPEpiC	eye:	n/a
11	chr8:4644719-4644769	Caco-2	colon:	n/a
12	chr8:4773213-4773263	AG10803	skin:	n/a
13	chr8:4644739-4644789	SK-N-MC	brain:	n/a
14	chr8:4629524-4629574	PANC-1	pancreas:	n/a
15	chr8:4773213-4773263	PANC-1	pancreas:	n/a
16	chr8:4617087-4617137	A549	lung:	n/a
17	chr8:4629524-4629574	HEEpiC	esophagus:	n/a
18	chr8:4773213-4773263	Hela-S3	cervix:	n/a
19	chr8:4644719-4644769	H1-hESC	embryonic stem cell:	embryo
20	chr8:4637584-4637634	Hela-S3	cervix:	n/a
21	chr8:4750513-4750563	AG10803	skin:	n/a
22	chr8:4617087-4617137	AG04450	lung:	fetal
23	chr8:4644739-4644789	HRE	kidney:	n/a
24	chr8:4629524-4629574	Caco-2	colon:	n/a
25	chr8:4629524-4629574	HCPEpiC	choroid plexus:	n/a
26	chr8:4750513-4750563	ovcar-3	ovarian:	n/a
27	chr8:4644739-4644789	HepG2	liver:	n/a
28	chr8:4773213-4773263	Hepatocyte	liver:	n/a
29	chr8:4629524-4629574	HL-60	blood:	n/a
30	chr8:4644719-4644769	LNCaP	prostate:	n/a
31	chr8:4637584-4637634	HIPEpiC	eye:	n/a
32	chr8:4644719-4644769	NHBE	bronchial:	n/a
33	chr8:4773213-4773263	NT2-D1	testis:	n/a
34	chr8:4773213-4773263	HUVEC	blood vessel:	n/a
35	chr8:4637584-4637634	HEK293	kidney:	embryo
36	chr8:4750513-4750563	AG09319	gingival:	n/a
37	chr8:4637584-4637634	RPTEC	kidney:	n/a
38	chr8:4617087-4617137	NT2-D1	testis:	n/a
39	chr8:4644719-4644769	AG09319	gingival:	n/a
40	chr8:4637584-4637634	ECC-1	luminal epithelium:	n/a
41	chr8:4644739-4644789	AG04449	skin:	fetal
42	chr8:4637584-4637634	BE2_C	brain:	n/a
43	chr8:4644719-4644769	PrEC	prostate:	n/a
44	chr8:4644739-4644789	T-47D	breast:	n/a
45	chr8:4617087-4617137	HRPEpiC	eye:	n/a
46	chr8:4644719-4644769	PANC-1	pancreas:	n/a
47	chr8:4617087-4617137	PrEC	prostate:	n/a
48	chr8:4773213-4773263	HEK293	kidney:	embryo
49	chr8:4644739-4644789	MCF10A-Er-Src	breast:	n/a
50	chr8:4617087-4617137	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4724555..4726658-chr8:4730823..4733487,2	K562	blood:
2	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
3	chr8:4696947..4699899-chr8:4702177..4705050,3	K562	blood:
4	chr8:4724555..4726658-chr8:4730823..4733487,2	K562	blood:
5	chr8:4696947..4699899-chr8:4702177..4705050,3	K562	blood:
6	chr8:4695059..4696118-chr8:4854167..4855161,8	MCF-7	breast:
7	chr8:4695207..4695958-chr8:4732618..4733342,2	MCF-7	breast:
8	chr8:4695207..4695958-chr8:4732618..4733342,2	MCF-7	breast:
9	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 7386 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:7386 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2407592	chr8:4610345-4610346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557776910	chr8:4610391-4610392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546251271	chr8:4610415-4610416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558600908	chr8:4610441-4610442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373289474	chr8:4610443-4610444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185780600	chr8:4610452-4610453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6558908	chr8:4610495-4610496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs187700883	chr8:4610500-4610501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533551482	chr8:4610504-4610505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192196411	chr8:4610508-4610509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6558909	chr8:4610510-4610511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs6994235	chr8:4610514-4610515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141644574	chr8:4610527-4610528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75184275	chr8:4610549-4610550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538896766	chr8:4610561-4610562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184508124	chr8:4610580-4610581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542336278	chr8:4610589-4610590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188873373	chr8:4610597-4610598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543260367	chr8:4610627-4610628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374364002	chr8:4610630-4610631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572546608	chr8:4610635-4610636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150531838	chr8:4610643-4610644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74503534	chr8:4610650-4610651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140441443	chr8:4610651-4610652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143989092	chr8:4610653-4610654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562655246	chr8:4610684-4610685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529953364	chr8:4610689-4610690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6558910	chr8:4610693-4610694	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566766917	chr8:4610698-4610699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6558911	chr8:4610703-4610704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184497858	chr8:4610705-4610706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554236337	chr8:4610723-4610724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147287038	chr8:4610735-4610736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376428081	chr8:4610742-4610743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77154177	chr8:4610759-4610760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557276325	chr8:4610763-4610764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140931100	chr8:4610767-4610768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545246779	chr8:4610791-4610792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13277205	chr8:4610813-4610814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs554891053	chr8:4610818-4610819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573181936	chr8:4610819-4610820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189509844	chr8:4610855-4610856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114072672	chr8:4610867-4610868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576887976	chr8:4610883-4610884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528026950	chr8:4610886-4610887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6558912	chr8:4610893-4610894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9657400	chr8:4610894-4610895	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs529944618	chr8:4610916-4610917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375252456	chr8:4610926-4610927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58730251	chr8:4610927-4610928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4593800-4616600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:4610600-4612600	Enhancers	Fetal Brain Male	brain
3	chr8:4611000-4611400	Enhancers	Stomach Smooth Muscle	stomach
4	chr8:4615000-4616800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:4616600-4617400	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:4616800-4617000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:4617000-4617200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr8:4617200-4617800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:4617400-4619600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:4617800-4619600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:4619600-4620200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:4619600-4620600	Enhancers	Brain Angular Gyrus	brain
13	chr8:4619600-4621000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:4619600-4623200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr8:4619800-4620400	Enhancers	Brain Hippocampus Middle	brain
16	chr8:4619800-4621000	Enhancers	Brain Substantia Nigra	brain
17	chr8:4620000-4620400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:4620000-4620400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:4620000-4620400	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr8:4620000-4621000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:4620200-4620600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:4620200-4620600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:4620200-4620600	Active TSS	Brain Anterior Caudate	brain
24	chr8:4620200-4620800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:4620400-4620800	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr8:4620400-4621000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr8:4620400-4621800	Enhancers	Brain Cingulate Gyrus	brain
28	chr8:4620600-4621000	Enhancers	Brain Anterior Caudate	brain
29	chr8:4620600-4621800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:4620600-4624000	Weak transcription	Brain Angular Gyrus	brain
31	chr8:4620800-4621000	Enhancers	Brain Hippocampus Middle	brain
32	chr8:4620800-4622200	Enhancers	Brain Germinal Matrix	brain
33	chr8:4621000-4630800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr8:4621800-4625000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:4623200-4625000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:4624800-4625200	ZNF genes & repeats	Brain Angular Gyrus	brain
37	chr8:4625000-4625200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
38	chr8:4625000-4625400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:4625200-4630600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr8:4625200-4631400	Weak transcription	Brain Angular Gyrus	brain
41	chr8:4628200-4629800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:4629800-4630800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:4630200-4630800	Enhancers	Brain Hippocampus Middle	brain
44	chr8:4630600-4630800	Enhancers	Brain Cingulate Gyrus	brain
45	chr8:4630800-4631200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:4630800-4631200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:4630800-4631200	Active TSS	Brain Anterior Caudate	brain
48	chr8:4630800-4631200	Active TSS	Brain Hippocampus Middle	brain
49	chr8:4630800-4631200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr8:4630800-4637000	Weak transcription	Brain Cingulate Gyrus	brain

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