Variant report

Variant	nsv465808
Chromosome Location	chr8:130963259-131118658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3725)
CpG islands
(count:1649)
Chromatin interactive
region (count:165)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:3725 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:131074225-131074884	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:131045172-131045208	K562	blood:	n/a	n/a
3	ARID3A	chr8:131054553-131055003	K562	blood:	n/a	n/a
4	ARID3A	chr8:131012944-131013054	K562	blood:	n/a	n/a
5	ARID3A	chr8:131014808-131014920	K562	blood:	n/a	n/a
6	ARID3A	chr8:131028825-131028876	K562	blood:	n/a	n/a
7	ARID3A	chr8:130983807-130984435	K562	blood:	n/a	n/a
8	ARID3A	chr8:131009008-131009301	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:130982576-130982644	K562	blood:	n/a	n/a
10	ARID3A	chr8:131027514-131028077	K562	blood:	n/a	n/a
11	ARID3A	chr8:131004638-131005192	K562	blood:	n/a	n/a
12	ARID3A	chr8:131106865-131107518	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:130985812-130985978	K562	blood:	n/a	n/a
14	ATF1	chr8:131054462-131054889	K562	blood:	n/a	n/a
15	ATF1	chr8:131080630-131081069	K562	blood:	n/a	n/a
16	ATF1	chr8:131114262-131114461	K562	blood:	n/a	n/a
17	ATF1	chr8:131117643-131117668	K562	blood:	n/a	n/a
18	ATF1	chr8:131004594-131005276	K562	blood:	n/a	n/a
19	ATF1	chr8:131044987-131045295	K562	blood:	n/a	n/a
20	ATF1	chr8:130985712-130985982	K562	blood:	n/a	n/a
21	ATF2	chr8:131054272-131055347	GM12878	blood:	n/a	n/a
22	ATF2	chr8:131027349-131027901	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr8:130983715-130984457	GM12878	blood:	n/a	n/a
24	ATF2	chr8:131027340-131027895	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:131020655-131021478	GM12878	blood:	n/a	n/a
26	ATF2	chr8:131041198-131041650	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr8:130996350-130996810	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr8:131020554-131021539	GM12878	blood:	n/a	n/a
29	ATF2	chr8:131048950-131049454	GM12878	blood:	n/a	n/a
30	ATF2	chr8:131091741-131092523	GM12878	blood:	n/a	n/a
31	ATF2	chr8:131054448-131055257	GM12878	blood:	n/a	n/a
32	ATF2	chr8:130983740-130984525	GM12878	blood:	n/a	n/a
33	ATF2	chr8:131091855-131092513	GM12878	blood:	n/a	n/a
34	ATF3	chr8:131054457-131054915	K562	blood:	n/a	n/a
35	ATF3	chr8:131012190-131012473	K562	blood:	n/a	n/a
36	ATF3	chr8:130996418-130996972	A549	lung:	n/a	n/a
37	ATF3	chr8:131008717-131009228	A549	lung:	n/a	n/a
38	ATF3	chr8:130996579-130996822	K562	blood:	n/a	n/a
39	ATF3	chr8:131027039-131028066	A549	lung:	n/a	chr8:131027168-131027181
40	ATF3	chr8:131012045-131012531	K562	blood:	n/a	n/a
41	ATF3	chr8:130996575-130996805	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr8:131044985-131045202	K562	blood:	n/a	n/a
43	ATF3	chr8:130996482-130996875	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF3	chr8:131044974-131045354	K562	blood:	n/a	n/a
45	ATF3	chr8:130983720-130984152	K562	blood:	n/a	n/a
46	BACH1	chr8:131006190-131006343	K562	blood:	n/a	n/a
47	BACH1	chr8:131009666-131009812	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr8:131054641-131054794	K562	blood:	n/a	chr8:131054710-131054724
49	BACH1	chr8:131004552-131005513	K562	blood:	n/a	n/a
50	BACH1	chr8:131011443-131012750	K562	blood:	n/a	chr8:131012319-131012333 chr8:131012309-131012323

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130992575-130992625	AoSMC	blood vessel:	n/a
2	chr8:131028985-131029035	SAEC	small airway:	n/a
3	chr8:130992575-130992625	AoSMC	blood vessel:	n/a
4	chr8:131028985-131029035	SAEC	small airway:	n/a
5	chr8:130995417-130995467	NT2-D1	testis:	n/a
6	chr8:131028990-131029040	ECC-1	luminal epithelium:	n/a
7	chr8:131080137-131080187	K562	blood:	n/a
8	chr8:130994109-130994159	HRPEpiC	eye:	n/a
9	chr8:131065129-131065179	ECC-1	luminal epithelium:	n/a
10	chr8:130996123-130996173	AG10803	skin:	n/a
11	chr8:131000415-131000465	HUVEC	blood vessel:	n/a
12	chr8:131028990-131029040	BE2_C	brain:	n/a
13	chr8:130998171-130998221	HCF	heart:	n/a
14	chr8:131011240-131011290	U87	brain:	n/a
15	chr8:131058332-131058382	HRCEpiC	kidney:	n/a
16	chr8:131025902-131025952	PANC-1	pancreas:	n/a
17	chr8:131075016-131075066	PFSK-1	brain:	n/a
18	chr8:130992575-130992625	Hela-S3	cervix:	n/a
19	chr8:131075016-131075066	SK-N-SH	brain:	n/a
20	chr8:131029139-131029189	PANC-1	pancreas:	n/a
21	chr8:131028985-131029035	HCT-116	colon:	n/a
22	chr8:130995997-130996047	CMK	blood:	n/a
23	chr8:131025902-131025952	ovcar-3	ovarian:	n/a
24	chr8:131080137-131080187	NH-A	brain:	n/a
25	chr8:131000261-131000311	ProgFib	skin:	n/a
26	chr8:131080137-131080187	HL-60	blood:	n/a
27	chr8:131028990-131029040	GM12892	blood:	n/a
28	chr8:131000415-131000465	Jurkat	blood:	n/a
29	chr8:131022097-131022147	MCF-7	breast:	n/a
30	chr8:130995990-130996040	SKMC	muscle:	n/a
31	chr8:131000261-131000311	MCF10A-Er-Src	breast:	n/a
32	chr8:131028232-131028282	HRE	kidney:	n/a
33	chr8:131028232-131028282	PrEC	prostate:	n/a
34	chr8:131058332-131058382	AG09319	gingival:	n/a
35	chr8:131000261-131000311	ECC-1	luminal epithelium:	n/a
36	chr8:130997672-130997722	GM12878	blood:	n/a
37	chr8:130996123-130996173	AG04449	skin:	fetal
38	chr8:130976125-130976175	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:131000415-131000465	SK-N-SH_RA	brain:	n/a
40	chr8:130994109-130994159	GM06990	blood:	n/a
41	chr8:131080137-131080187	AoSMC	blood vessel:	n/a
42	chr8:131031752-131031802	T-47D	breast:	n/a
43	chr8:131028232-131028282	PANC-1	pancreas:	n/a
44	chr8:131054408-131054458	HEEpiC	esophagus:	n/a
45	chr8:131000415-131000465	PFSK-1	brain:	n/a
46	chr8:131029139-131029189	Jurkat	blood:	n/a
47	chr8:130992575-130992625	A549	lung:	n/a
48	chr8:131027724-131027774	HCF	heart:	n/a
49	chr8:131080137-131080187	HRPEpiC	eye:	n/a
50	chr8:131054408-131054458	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:130949866..130952104-chr8:131031388..131034166,2	K562	blood:
2	chr8:130981588..130985969-chr8:131024671..131030870,8	K562	blood:
3	chr8:131032809..131035482-chr8:131037784..131039457,2	K562	blood:
4	chr8:130981588..130985969-chr8:131027661..131030801,4	K562	blood:
5	chr8:130975214..130976755-chr8:130983045..130985731,2	MCF-7	breast:
6	chr8:130967769..130969893-chr8:131027217..131029473,2	K562	blood:
7	chr8:130974926..130980005-chr8:130980805..130983259,5	K562	blood:
8	chr8:130951528..130952250-chr8:131028470..131029127,2	MCF-7	breast:
9	chr8:131021262..131023800-chr8:131023935..131026265,2	MCF-7	breast:
10	chr8:130982299..130983095-chr8:131026665..131027754,4	MCF-7	breast:
11	chr8:130996585..131001100-chr8:131002410..131006763,8	K562	blood:
12	chr8:131052756..131054836-chr8:131056637..131059542,2	K562	blood:
13	chr8:131096532..131098102-chr8:131100049..131102503,2	K562	blood:
14	chr8:131056726..131059122-chr8:131059475..131061608,2	K562	blood:
15	chr8:131057701..131060248-chr8:131066752..131069472,2	K562	blood:
16	chr8:131067228..131068888-chr8:131073301..131075173,2	K562	blood:
17	chr8:131017010..131019589-chr8:131030192..131032616,2	K562	blood:
18	chr12:11801638..11802342-chr8:131054390..131055145,2	Hela-S3	cervix:
19	chr8:130996752..130999185-chr8:131000348..131002341,2	MCF-7	breast:
20	chr8:130966871..130968440-chr8:130972283..130975022,2	K562	blood:
21	chr8:131007021..131009238-chr8:131011453..131013766,3	MCF-7	breast:
22	chr8:130994427..130996216-chr8:130998124..131000537,2	MCF-7	breast:
23	chr8:130949745..130951493-chr8:130983893..130985842,2	K562	blood:
24	chr8:130995016..130997568-chr8:131000713..131003679,2	MCF-7	breast:
25	chr8:131099858..131101381-chr8:131107390..131110366,2	K562	blood:
26	chr8:131076275..131077989-chr8:131079170..131082026,2	K562	blood:
27	chr8:130965774..130967791-chr8:130974900..130977591,2	K562	blood:
28	chr8:130950293..130952850-chr8:131027033..131029151,3	MCF-7	breast:
29	chr8:130954709..130956974-chr8:130965501..130967949,2	K562	blood:
30	chr8:131027480..131030548-chr8:131053151..131055145,3	K562	blood:
31	chr8:130986305..130988382-chr8:130992226..130994888,2	K562	blood:
32	chr8:131023287..131025131-chr8:131027494..131029690,2	MCF-7	breast:
33	chr8:130974170..130976536-chr8:130978429..130983259,4	K562	blood:
34	chr8:131045657..131048618-chr8:131053552..131056058,2	K562	blood:
35	chr8:130995016..130997568-chr8:131000713..131003679,2	MCF-7	breast:
36	chr8:131027601..131029228-chr8:131030030..131032966,2	MCF-7	breast:
37	chr8:130994883..130996522-chr8:131001539..131003623,2	K562	blood:
38	chr8:131028813..131030509-chr8:131031181..131032735,2	MCF-7	breast:
39	chr8:130973733..130976388-chr8:130984110..130986683,2	K562	blood:
40	chr8:130951997..130952639-chr8:131027123..131027922,3	MCF-7	breast:
41	chr20:47442643..47444706-chr8:131026917..131028434,2	MCF-7	breast:
42	chr8:131062555..131064822-chr8:131096828..131099567,2	K562	blood:
43	chr8:131044244..131046702-chr8:131056220..131058655,2	MCF-7	breast:
44	chr8:130994958..130999216-chr8:131005349..131009996,7	MCF-7	breast:
45	chr8:130965774..130967791-chr8:130974900..130977591,2	K562	blood:
46	chr8:131052756..131054836-chr8:131056637..131059542,2	K562	blood:
47	chr8:131003704..131005230-chr8:131007280..131008801,2	K562	blood:
48	chr8:131035060..131037464-chr8:131038992..131041654,2	K562	blood:
49	chr8:131027127..131029868-chr8:131056253..131058573,2	MCF-7	breast:
50	chr8:130974580..130976381-chr8:130980211..130982416,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM49B-2	chr8:131094984-131097014	NONHSAT129148
2	lnc-GSDMC-5	chr8:131028853-131028898	NONHSAT129141
3	lnc-EFR3A-10	chr8:131085393-131085648	NONHSAT129146
4	lnc-GSDMC-5	chr8:130982755-130983241	NONHSAT129141

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5194	chr8:131020606-131020627	MIMAT0021125

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ASAP1	hsa-miR-98-5p	chr8:131066295-131066316

Variant related genes	Relation type
RNU6-1255P	TF binding region
RNU7-181P	TF binding region
MIR5194	TF binding region
FAM49B	TF binding region
ENSG00000203377	TF binding region
RNU6-1255P	CpG island
RNU7-181P	CpG island
MIR5194	CpG island
FAM49B	CpG island
ENSG00000203377	CpG island
ENSG00000153317	chromatin interactions
ENSG00000253720	chromatin interactions
ENSG00000200304	chromatin interactions
ENSG00000253043	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000153310	chromatin interactions
ENSG00000264653	chromatin interactions

Extended variants
information (count: 6163 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:6163 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1670745	chr8:130963259-130963260	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544981266	chr8:130963288-130963289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563319394	chr8:130963330-130963331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190440622	chr8:130963334-130963335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182218592	chr8:130963335-130963336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561431781	chr8:130963367-130963368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528705450	chr8:130963371-130963372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143287751	chr8:130963377-130963378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571721967	chr8:130963418-130963419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540309907	chr8:130963419-130963420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148325950	chr8:130963442-130963443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568947577	chr8:130963443-130963444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185962093	chr8:130963469-130963470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555265795	chr8:130963494-130963495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567303476	chr8:130963495-130963496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534827629	chr8:130963499-130963500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189891685	chr8:130963515-130963516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577665785	chr8:130963526-130963527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544803643	chr8:130963566-130963567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529820232	chr8:130963602-130963603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114695855	chr8:130963608-130963609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141915257	chr8:130963631-130963632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543314540	chr8:130963649-130963650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180804930	chr8:130963657-130963658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71572305	chr8:130963673-130963674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200323460	chr8:130963683-130963684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371017305	chr8:130963686-130963687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540808821	chr8:130963690-130963691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201489510	chr8:130963704-130963705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565383918	chr8:130963724-130963725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532626027	chr8:130963737-130963738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550680508	chr8:130963749-130963750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562517709	chr8:130963782-130963783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185604432	chr8:130963808-130963809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571053024	chr8:130963813-130963814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538367166	chr8:130963827-130963828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113171376	chr8:130963829-130963830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190022057	chr8:130963876-130963877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546752619	chr8:130963877-130963878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555590145	chr8:130963928-130963929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35141996	chr8:130963952-130963953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73398748	chr8:130963995-130963996	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556677130	chr8:130964025-130964026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572136538	chr8:130964034-130964035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557113874	chr8:130964047-130964048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575262540	chr8:130964050-130964051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568481214	chr8:130964058-130964059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536260376	chr8:130964068-130964069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182957458	chr8:130964074-130964075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539346232	chr8:130964092-130964093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Schizophrenia	23813976	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:6072 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130952600-130965600	Weak transcription	Aorta	Aorta
2	chr8:130952600-130965600	Weak transcription	Lung	lung
3	chr8:130952800-130965200	Weak transcription	Colonic Mucosa	Colon
4	chr8:130952800-130965400	Weak transcription	Gastric	stomach
5	chr8:130952800-130965400	Weak transcription	Pancreas	Pancrea
6	chr8:130952800-130965400	Weak transcription	Psoas Muscle	Psoas
7	chr8:130952800-130965400	Weak transcription	HSMMtube	muscle
8	chr8:130952800-130967800	Weak transcription	Right Ventricle	heart
9	chr8:130952800-130981400	Weak transcription	Left Ventricle	heart
10	chr8:130953000-130965000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr8:130953000-130967400	Weak transcription	Fetal Stomach	stomach
12	chr8:130953000-130980000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:130953200-130964800	Weak transcription	Brain Substantia Nigra	brain
14	chr8:130953200-130968800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr8:130953200-130969200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr8:130953200-130970400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:130953200-130974800	Weak transcription	Fetal Brain Female	brain
18	chr8:130953400-130965200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr8:130953400-130965200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr8:130953400-130968800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr8:130953400-130969000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr8:130953400-130969400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr8:130953400-130970400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:130953400-130982000	Weak transcription	Hela-S3	cervix
25	chr8:130953600-130975400	Weak transcription	HMEC	breast
26	chr8:130953600-130980000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr8:130958200-130965400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr8:130958200-130965600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:130958600-130965400	Weak transcription	Placenta	Placenta
30	chr8:130958800-130965000	Weak transcription	Brain Hippocampus Middle	brain
31	chr8:130959000-130964800	Weak transcription	Brain Anterior Caudate	brain
32	chr8:130959200-130979400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr8:130959200-130982200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr8:130959200-130983400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr8:130959400-130965400	Weak transcription	Fetal Intestine Small	intestine
36	chr8:130959600-130969400	Strong transcription	Primary B cells from peripheral blood	blood
37	chr8:130959800-130965600	Weak transcription	Fetal Intestine Large	intestine
38	chr8:130960200-130965600	Weak transcription	K562	blood
39	chr8:130960600-130969400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr8:130960800-130965000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr8:130960800-130965200	Weak transcription	Brain Angular Gyrus	brain
42	chr8:130960800-130965200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr8:130960800-130965200	Weak transcription	A549	lung
44	chr8:130960800-130965400	Weak transcription	Fetal Muscle Leg	muscle
45	chr8:130960800-130965600	Weak transcription	Adipose Nuclei	Adipose
46	chr8:130961000-130964800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr8:130961000-130965200	Weak transcription	Spleen	Spleen
48	chr8:130961000-130965600	Weak transcription	Esophagus	oesophagus
49	chr8:130961000-130968800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr8:130961000-130970400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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