Variant report

Variant	nsv1019536
Chromosome Location	chr8:11788237-11828263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1241)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
4	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
5	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
6	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
7	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
8	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
12	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
14	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
15	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
16	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372
17	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
18	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
19	BHLHE40	chr8:11799584-11800147	K562	blood:	n/a	n/a
20	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372
21	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
22	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
23	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
24	BRCA1	chr8:11801202-11801448	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr8:11801145-11801480	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr8:11796176-11796816	K562	blood:	n/a	n/a
27	CBX3	chr8:11805093-11805433	K562	blood:	n/a	n/a
28	CBX3	chr8:11796463-11796779	K562	blood:	n/a	n/a
29	CBX3	chr8:11799688-11800155	K562	blood:	n/a	n/a
30	CCNT2	chr8:11807053-11807488	K562	blood:	n/a	chr8:11807360-11807369 chr8:11807248-11807268
31	CCNT2	chr8:11799474-11800136	K562	blood:	n/a	n/a
32	CEBPB	chr8:11813778-11814109	A549	lung:	n/a	chr8:11813929-11813940
33	CEBPB	chr8:11795384-11795418	HepG2	liver:	n/a	chr8:11795407-11795418
34	CEBPB	chr8:11813825-11814061	K562	blood:	n/a	chr8:11813929-11813940
35	CEBPB	chr8:11813757-11814093	K562	blood:	n/a	chr8:11813929-11813940
36	CEBPB	chr8:11813814-11814090	A549	lung:	n/a	chr8:11813929-11813940
37	CEBPB	chr8:11816146-11816527	MCF-7	breast:	n/a	chr8:11816330-11816341
38	CEBPB	chr8:11816229-11816539	HepG2	liver:	n/a	chr8:11816330-11816341
39	CEBPB	chr8:11795337-11795460	IMR90	lung:	n/a	chr8:11795407-11795418
40	CEBPB	chr8:11816146-11816622	A549	lung:	n/a	chr8:11816330-11816341
41	CEBPB	chr8:11813744-11814114	HepG2	liver:	n/a	chr8:11813929-11813940
42	CEBPB	chr8:11816261-11816393	HepG2	liver:	n/a	chr8:11816330-11816341
43	CEBPB	chr8:11816175-11816712	K562	blood:	n/a	chr8:11816330-11816341
44	CEBPB	chr8:11813778-11814105	IMR90	lung:	n/a	chr8:11813929-11813940
45	CEBPB	chr8:11816235-11816570	ECC-1	luminal epithelium:	n/a	chr8:11816330-11816341
46	CEBPB	chr8:11816251-11816631	H1-hESC	embryonic stem cell:	n/a	chr8:11816330-11816341
47	CEBPB	chr8:11813806-11814094	Hela-S3	cervix:	n/a	chr8:11813929-11813940
48	CEBPB	chr8:11821309-11821507	HepG2	liver:	n/a	chr8:11821395-11821406
49	CEBPB	chr8:11816165-11816600	A549	lung:	n/a	chr8:11816330-11816341
50	CEBPB	chr8:11795283-11795462	A549	lung:	n/a	chr8:11795407-11795418

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11790326-11790376	HEEpiC	esophagus:	n/a
2	chr8:11801320-11801370	U87	brain:	n/a
3	chr8:11790326-11790376	HCF	heart:	n/a
4	chr8:11795273-11795323	HIPEpiC	eye:	n/a
5	chr8:11801320-11801370	HepG2	liver:	n/a
6	chr8:11790559-11790609	BJ	skin:	n/a
7	chr8:11813211-11813261	Hela-S3	cervix:	n/a
8	chr8:11801320-11801370	Hepatocyte	liver:	n/a
9	chr8:11790559-11790609	GM12878	blood:	n/a
10	chr8:11801320-11801370	IMR90	lung:	fetal
11	chr8:11794716-11794766	T-47D	breast:	n/a
12	chr8:11790559-11790609	PFSK-1	brain:	n/a
13	chr8:11801365-11801415	HL-60	blood:	n/a
14	chr8:11801320-11801370	AoSMC	blood vessel:	n/a
15	chr8:11795273-11795323	Jurkat	blood:	n/a
16	chr8:11813211-11813261	Caco-2	colon:	n/a
17	chr8:11801365-11801415	U87	brain:	n/a
18	chr8:11801320-11801370	HEEpiC	esophagus:	n/a
19	chr8:11801320-11801370	SAEC	small airway:	n/a
20	chr8:11801320-11801370	HEK293	kidney:	embryo
21	chr8:11801320-11801370	AG09319	gingival:	n/a
22	chr8:11801365-11801415	HCF	heart:	n/a
23	chr8:11794950-11795000	MCF-7	breast:	n/a
24	chr8:11801320-11801370	GM12878	blood:	n/a
25	chr8:11801320-11801370	K562	blood:	n/a
26	chr8:11795273-11795323	GM12891	blood:	n/a
27	chr8:11795262-11795312	HUVEC	blood vessel:	n/a
28	chr8:11801365-11801415	SK-N-MC	brain:	n/a
29	chr8:11801365-11801415	HMEC	breast:	n/a
30	chr8:11794716-11794766	Jurkat	blood:	n/a
31	chr8:11801365-11801415	PANC-1	pancreas:	n/a
32	chr8:11790639-11790689	NH-A	brain:	n/a
33	chr8:11790559-11790609	H1-hESC	embryonic stem cell:	embryo
34	chr8:11794716-11794766	NH-A	brain:	n/a
35	chr8:11813211-11813261	AoSMC	blood vessel:	n/a
36	chr8:11795262-11795312	HCT-116	colon:	n/a
37	chr8:11801320-11801370	H1-hESC	embryonic stem cell:	embryo
38	chr8:11801365-11801415	PFSK-1	brain:	n/a
39	chr8:11794716-11794766	CMK	blood:	n/a
40	chr8:11795262-11795312	SKMC	muscle:	n/a
41	chr8:11794950-11795000	HIPEpiC	eye:	n/a
42	chr8:11801320-11801370	T-47D	breast:	n/a
43	chr8:11794950-11795000	HUVEC	blood vessel:	n/a
44	chr8:11790559-11790609	GM06990	blood:	n/a
45	chr8:11794950-11795000	NHBE	bronchial:	n/a
46	chr8:11813211-11813261	K562	blood:	n/a
47	chr8:11794716-11794766	Caco-2	colon:	n/a
48	chr8:11795273-11795323	SK-N-SH_RA	brain:	n/a
49	chr8:11794716-11794766	HEEpiC	esophagus:	n/a
50	chr8:11795273-11795323	NHBE	bronchial:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
2	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:
3	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
4	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
5	chr8:11723911..11726339-chr8:11798413..11801274,2	K562	blood:
6	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
7	chr8:11622652..11623752-chr8:11800899..11801806,5	MCF-7	breast:
8	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
9	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
10	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
11	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
12	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
13	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
14	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
15	chr8:11710424..11713168-chr8:11798660..11801424,2	K562	blood:
16	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
17	chr8:11619764..11620442-chr8:11816053..11817012,3	K562	blood:
18	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
19	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
20	chr8:11622669..11623564-chr8:11800869..11801753,3	K562	blood:
21	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
22	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
23	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
24	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
25	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
26	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
27	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
28	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
29	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
30	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:

No data

Variant related genes	Relation type
OR7E161P	TF binding region
OR7E161P	CpG island
ENSG00000255046	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000164733	chromatin interactions

Extended variants
information (count: 2647 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2647 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200921313	chr8:11788238-11788239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62493600	chr8:11788251-11788252	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
3	rs62493601	chr8:11788307-11788308	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs185589036	chr8:11788313-11788314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs58048489	chr8:11788352-11788353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557456634	chr8:11788362-11788363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527961909	chr8:11788369-11788370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549579160	chr8:11788392-11788393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187672838	chr8:11788406-11788407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150136871	chr8:11788464-11788465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs58049869	chr8:11788495-11788496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs192116729	chr8:11788500-11788501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184373658	chr8:11788507-11788508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557315910	chr8:11788515-11788516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61055172	chr8:11788548-11788549	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs540153724	chr8:11788550-11788551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61641133	chr8:11788556-11788557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555576943	chr8:11788610-11788611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367770347	chr8:11788623-11788624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544347411	chr8:11788624-11788625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562992225	chr8:11788638-11788639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533427954	chr8:11788642-11788643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545450107	chr8:11788660-11788661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs58325983	chr8:11788663-11788664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs528031034	chr8:11788664-11788665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549423024	chr8:11788674-11788675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59423463	chr8:11788694-11788695	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs531835879	chr8:11788706-11788707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368692314	chr8:11788707-11788708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549929219	chr8:11788712-11788713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568646664	chr8:11788743-11788744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539125950	chr8:11788786-11788787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557379402	chr8:11788791-11788792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188695125	chr8:11788801-11788802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79488203	chr8:11788803-11788804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372292765	chr8:11788824-11788825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555376364	chr8:11788861-11788862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377148582	chr8:11788862-11788863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181181290	chr8:11788869-11788870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538051265	chr8:11788873-11788874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184412343	chr8:11788876-11788877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189395460	chr8:11788883-11788884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368246222	chr8:11788890-11788891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560532605	chr8:11788913-11788914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572354268	chr8:11788915-11788916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542981624	chr8:11788921-11788922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199830448	chr8:11788932-11788933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200493256	chr8:11788934-11788935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182241422	chr8:11788936-11788937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532016003	chr8:11788960-11788961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11786000-11799400	Weak transcription	Right Atrium	heart
2	chr8:11786600-11788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:11786800-11790600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:11787000-11790600	Weak transcription	NHEK	skin
5	chr8:11789200-11789400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:11790600-11790800	Enhancers	Placenta	Placenta
7	chr8:11790600-11791400	Enhancers	NHEK	skin
8	chr8:11790600-11791600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:11791000-11791200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:11791200-11791400	Enhancers	HepG2	liver
11	chr8:11791200-11791600	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr8:11791200-11792200	Enhancers	Pancreas	Pancrea
13	chr8:11791200-11792200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr8:11791200-11793600	Enhancers	Duodenum Mucosa	Duodenum
15	chr8:11791400-11791600	Enhancers	Placenta	Placenta
16	chr8:11791400-11791800	Enhancers	K562	blood
17	chr8:11791400-11792000	Flanking Active TSS	HepG2	liver
18	chr8:11791400-11792200	Enhancers	Fetal Intestine Small	intestine
19	chr8:11791400-11793200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr8:11791400-11793600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:11791400-11794200	Enhancers	Stomach Mucosa	stomach
22	chr8:11791600-11792800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:11791800-11792000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:11791800-11793400	Weak transcription	K562	blood
25	chr8:11792000-11793600	Enhancers	HepG2	liver
26	chr8:11792000-11794000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:11792200-11793600	Weak transcription	Fetal Intestine Small	intestine
28	chr8:11793000-11793400	Enhancers	Gastric	stomach
29	chr8:11793000-11794000	Enhancers	Primary hematopoietic stem cells	blood
30	chr8:11793200-11793400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:11793200-11793600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr8:11793200-11793800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
33	chr8:11793200-11793800	Bivalent Enhancer	Small Intestine	intestine
34	chr8:11793200-11794200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
35	chr8:11793200-11794200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:11793400-11793600	Enhancers	K562	blood
37	chr8:11793400-11793800	Enhancers	Esophagus	oesophagus
38	chr8:11793400-11794000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:11793600-11793800	Enhancers	Fetal Intestine Small	intestine
40	chr8:11793600-11793800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
41	chr8:11793600-11794200	Enhancers	A549	lung
42	chr8:11793600-11794200	Weak transcription	K562	blood
43	chr8:11793800-11794000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr8:11794000-11794200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:11794200-11794400	Enhancers	K562	blood
46	chr8:11794200-11798800	Weak transcription	Stomach Mucosa	stomach
47	chr8:11797400-11798800	Weak transcription	Fetal Intestine Small	intestine
48	chr8:11798600-11798800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr8:11798600-11799800	Enhancers	K562	blood
50	chr8:11798600-11800200	Enhancers	Fetal Heart	heart

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