Variant report

Variant	nsv539458
Chromosome Location	chr8:8522963-8565946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1317)
CpG islands
(count:793)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8527251-8527584	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8528189-8528428	K562	blood:	n/a	n/a
3	ATF2	chr8:8564374-8564717	GM12878	blood:	n/a	n/a
4	BACH1	chr8:8537468-8538147	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:8564710-8564764	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:8537583-8538057	K562	blood:	n/a	n/a
7	BACH1	chr8:8559169-8559350	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr8:8559115-8559431	GM12878	blood:	n/a	n/a
9	BCLAF1	chr8:8527098-8527576	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:8527123-8527512	GM12878	blood:	n/a	n/a
11	BCLAF1	chr8:8564353-8564640	GM12878	blood:	n/a	chr8:8564481-8564490
12	BHLHE40	chr8:8528152-8528406	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:8559215-8559478	HepG2	liver:	n/a	n/a
14	BHLHE40	chr8:8540163-8540328	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:8559150-8559442	K562	blood:	n/a	n/a
16	BHLHE40	chr8:8537732-8538123	K562	blood:	n/a	n/a
17	BHLHE40	chr8:8559193-8559537	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:8554817-8555130	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:8528149-8528326	K562	blood:	n/a	n/a
20	BRCA1	chr8:8527130-8527557	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr8:8539713-8540057	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:8559047-8559407	K562	blood:	n/a	n/a
23	CCNT2	chr8:8559110-8559705	K562	blood:	n/a	chr8:8559404-8559413
24	CEBPB	chr8:8562153-8562423	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:8527207-8527577	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:8534516-8534769	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:8527094-8527569	A549	lung:	n/a	n/a
28	CEBPB	chr8:8534509-8534744	K562	blood:	n/a	n/a
29	CEBPB	chr8:8537870-8538059	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:8537767-8538171	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:8554573-8554698	K562	blood:	n/a	chr8:8554639-8554650
32	CEBPB	chr8:8534608-8534691	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:8537839-8538093	A549	lung:	n/a	n/a
34	CEBPB	chr8:8556244-8556412	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:8527242-8527504	A549	lung:	n/a	n/a
36	CEBPB	chr8:8554530-8554742	HepG2	liver:	n/a	chr8:8554639-8554650
37	CEBPB	chr8:8559238-8559350	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:8539766-8540140	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:8527289-8527522	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:8539801-8540121	HCT-116	colon:	n/a	n/a
41	CEBPD	chr8:8559278-8559538	HepG2	liver:	n/a	n/a
42	CHD2	chr8:8554873-8554960	GM12878	blood:	n/a	n/a
43	CHD2	chr8:8562079-8562511	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr8:8559022-8559523	Hela-S3	cervix:	n/a	chr8:8559405-8559415
45	CHD2	chr8:8559358-8559619	GM12878	blood:	n/a	chr8:8559516-8559526 chr8:8559405-8559415
46	CHD2	chr8:8559059-8559935	H1-hESC	embryonic stem cell:	n/a	chr8:8559516-8559526 chr8:8559405-8559415
47	CHD2	chr8:8540211-8540312	GM12878	blood:	n/a	n/a
48	CREB1	chr8:8559023-8559733	A549	lung:	n/a	n/a
49	CREB1	chr8:8559681-8560152	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr8:8559021-8559561	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8559132-8559182	GM12891	blood:	n/a
2	chr8:8559461-8559511	Caco-2	colon:	n/a
3	chr8:8560934-8560984	HCT-116	colon:	n/a
4	chr8:8560866-8560916	GM12892	blood:	n/a
5	chr8:8559673-8559723	Caco-2	colon:	n/a
6	chr8:8559678-8559728	Hepatocyte	liver:	n/a
7	chr8:8559461-8559511	AG10803	skin:	n/a
8	chr8:8560427-8560477	U87	brain:	n/a
9	chr8:8559678-8559728	HAEpiC	amniotic membrane:	n/a
10	chr8:8559259-8559309	BJ	skin:	n/a
11	chr8:8559673-8559723	HEK293	kidney:	embryo
12	chr8:8559673-8559723	GM12892	blood:	n/a
13	chr8:8559999-8560049	SK-N-SH	brain:	n/a
14	chr8:8560934-8560984	SKMC	muscle:	n/a
15	chr8:8560866-8560916	AG04450	lung:	fetal
16	chr8:8559461-8559511	Hepatocyte	liver:	n/a
17	chr8:8559461-8559511	T-47D	breast:	n/a
18	chr8:8559673-8559723	HRE	kidney:	n/a
19	chr8:8563747-8563797	T-47D	breast:	n/a
20	chr8:8537351-8537401	MCF10A-Er-Src	breast:	n/a
21	chr8:8559259-8559309	PrEC	prostate:	n/a
22	chr8:8537351-8537401	HL-60	blood:	n/a
23	chr8:8560427-8560477	GM12892	blood:	n/a
24	chr8:8560934-8560984	IMR90	lung:	fetal
25	chr8:8559673-8559723	SK-N-SH_RA	brain:	n/a
26	chr8:8559999-8560049	GM12892	blood:	n/a
27	chr8:8559999-8560049	AG04449	skin:	fetal
28	chr8:8560866-8560916	Jurkat	blood:	n/a
29	chr8:8563747-8563797	Jurkat	blood:	n/a
30	chr8:8563747-8563797	HL-60	blood:	n/a
31	chr8:8563747-8563797	Hepatocyte	liver:	n/a
32	chr8:8559999-8560049	SKMC	muscle:	n/a
33	chr8:8537351-8537401	AG09309	skin:	n/a
34	chr8:8560866-8560916	HUVEC	blood vessel:	n/a
35	chr8:8555344-8555394	K562	blood:	n/a
36	chr8:8555344-8555394	AG09309	skin:	n/a
37	chr8:8559132-8559182	HAEpiC	amniotic membrane:	n/a
38	chr8:8559074-8559124	NHBE	bronchial:	n/a
39	chr8:8559259-8559309	PANC-1	pancreas:	n/a
40	chr8:8537351-8537401	Jurkat	blood:	n/a
41	chr8:8559132-8559182	Hela-S3	cervix:	n/a
42	chr8:8559132-8559182	PrEC	prostate:	n/a
43	chr8:8559461-8559511	SKMC	muscle:	n/a
44	chr8:8560934-8560984	GM12891	blood:	n/a
45	chr8:8560934-8560984	PrEC	prostate:	n/a
46	chr8:8559074-8559124	GM06990	blood:	n/a
47	chr8:8559461-8559511	HRCEpiC	kidney:	n/a
48	chr8:8559678-8559728	A549	lung:	n/a
49	chr8:8555344-8555394	HCF	heart:	n/a
50	chr8:8560934-8560984	HAEpiC	amniotic membrane:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8517125..8519695-chr8:8524278..8527180,2	MCF-7	breast:
2	chr8:8556386..8558383-chr8:8560900..8563538,2	K562	blood:
3	chr8:8527493..8529178-chr8:8594079..8595134,11	MCF-7	breast:
4	chr8:8521708..8523657-chr8:8525463..8527209,2	MCF-7	breast:
5	chr8:8563551..8565890-chr8:8569428..8571116,2	K562	blood:
6	chr8:8553109..8555242-chr8:8558598..8560731,2	MCF-7	breast:
7	chr8:8532775..8534463-chr8:8543028..8544705,2	MCF-7	breast:
8	chr8:8527809..8528658-chr8:8569477..8570252,2	MCF-7	breast:
9	chr8:8527839..8528754-chr8:8592246..8592999,2	K562	blood:
10	chr8:8241176..8241736-chr8:8524635..8525188,2	MCF-7	breast:
11	chr8:8538997..8539534-chr8:8594174..8595039,2	MCF-7	breast:
12	chr8:8556386..8558383-chr8:8560900..8563538,2	K562	blood:
13	chr15:56285724..56286656-chr8:8559373..8559873,2	Hela-S3	cervix:
14	chr8:8527332..8529283-chr8:8594084..8595110,9	K562	blood:
15	chr8:8455617..8458254-chr8:8522777..8525195,2	MCF-7	breast:
16	chr8:8521708..8523657-chr8:8525463..8527209,2	MCF-7	breast:
17	chr8:8553226..8556449-chr8:8563078..8566145,3	MCF-7	breast:
18	chr8:8130384..8131365-chr8:8526780..8528280,9	K562	blood:
19	chr8:8553226..8556449-chr8:8563078..8566145,3	MCF-7	breast:
20	chr8:8559280..8561948-chr8:8563852..8566020,2	MCF-7	breast:
21	chr8:8557473..8560405-chr8:8562361..8564009,2	K562	blood:
22	chr8:8536305..8538108-chr8:8559326..8560913,2	MCF-7	breast:
23	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
24	chr8:8558568..8560739-chr8:8564922..8567226,2	MCF-7	breast:
25	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
26	chr8:8560907..8563057-chr8:8567449..8569715,2	MCF-7	breast:
27	chr8:8528173..8528908-chr8:8567698..8568456,2	MCF-7	breast:
28	chr8:8527857..8528805-chr8:9688247..9689065,2	K562	blood:
29	chr8:8130322..8131342-chr8:8527334..8528198,3	MCF-7	breast:
30	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
31	chr8:8527797..8529806-chr8:8592444..8595839,3	MCF-7	breast:
32	chr8:8129344..8132133-chr8:8525629..8527896,2	MCF-7	breast:
33	chr8:8532775..8534463-chr8:8543028..8544705,2	MCF-7	breast:
34	chr8:8528265..8529882-chr8:8531395..8534062,2	MCF-7	breast:
35	chr8:8528265..8529882-chr8:8531395..8534062,2	MCF-7	breast:
36	chr8:8242334..8244521-chr8:8525850..8528752,3	MCF-7	breast:
37	chr8:8559423..8561174-chr8:8562199..8564616,2	MCF-7	breast:

No data

Variant related genes	Relation type
CLDN23	TF binding region
ENSG00000176305	TF binding region
CLDN23	CpG island
ENSG00000176305	CpG island
ENSG00000176305	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000182319	chromatin interactions
ENSG00000069869	chromatin interactions

Extended variants
information (count: 2523 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:2523 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528234603	chr8:8522974-8522975	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs566168220	chr8:8523020-8523021	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs78964173	chr8:8523023-8523024	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs557896690	chr8:8523060-8523061	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs577737275	chr8:8523066-8523067	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs148138331	chr8:8523077-8523078	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs185728790	chr8:8523084-8523085	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs9693402	chr8:8523158-8523159	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs541807480	chr8:8523170-8523171	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs367670988	chr8:8523177-8523178	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs572184812	chr8:8523179-8523180	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs541247474	chr8:8523218-8523219	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs11991078	chr8:8523227-8523228	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs533067177	chr8:8523239-8523240	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs561404230	chr8:8523294-8523295	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs370862497	chr8:8523323-8523324	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs563182377	chr8:8523327-8523328	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs117870861	chr8:8523336-8523337	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs368324778	chr8:8523341-8523342	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs549445181	chr8:8523348-8523349	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs530439901	chr8:8523362-8523363	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs374728380	chr8:8523367-8523368	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs566377667	chr8:8523376-8523377	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs372261002	chr8:8523393-8523394	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs534957921	chr8:8523404-8523405	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs551561814	chr8:8523415-8523416	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs141917581	chr8:8523451-8523452	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs116146791	chr8:8523459-8523460	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77092272	chr8:8523472-8523473	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs190642798	chr8:8523480-8523481	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs181742762	chr8:8523488-8523489	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183666235	chr8:8523502-8523503	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs188035128	chr8:8523526-8523527	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147259982	chr8:8523538-8523539	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs140720902	chr8:8523544-8523545	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577906767	chr8:8523556-8523557	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs371569995	chr8:8523591-8523592	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs377283216	chr8:8523599-8523600	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs570836239	chr8:8523608-8523609	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528947666	chr8:8523625-8523626	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs542629947	chr8:8523649-8523650	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs559040908	chr8:8523660-8523661	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567034792	chr8:8523663-8523664	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533442441	chr8:8523677-8523678	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs547219364	chr8:8523692-8523693	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs377247194	chr8:8523708-8523709	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528770578	chr8:8523721-8523722	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181283077	chr8:8523735-8523736	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566957329	chr8:8523745-8523746	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571557960	chr8:8523778-8523779	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
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
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
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
Colorectal cancer	16774939	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
Bladder cancer	21909424	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
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8514200-8527000	Weak transcription	Fetal Kidney	kidney
2	chr8:8521000-8524800	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr8:8521000-8525000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:8521400-8523200	Enhancers	Placenta	Placenta
5	chr8:8521600-8523000	Bivalent Enhancer	Fetal Heart	heart
6	chr8:8521600-8523600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr8:8521600-8523600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:8521600-8524600	Enhancers	Fetal Brain Male	brain
9	chr8:8521600-8525000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:8521800-8523400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr8:8521800-8523400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:8521800-8523600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:8522000-8523000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr8:8522000-8523200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr8:8522000-8523400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr8:8522000-8523600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:8522000-8523800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:8522000-8523800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr8:8522000-8524000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:8522200-8523200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:8522200-8523200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:8522200-8523200	Enhancers	Fetal Muscle Leg	muscle
23	chr8:8522200-8523200	Flanking Active TSS	NHEK	skin
24	chr8:8522200-8523400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:8522200-8523400	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr8:8522200-8523400	Flanking Active TSS	NH-A	brain
27	chr8:8522200-8523600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:8522200-8527000	Weak transcription	HepG2	liver
29	chr8:8522400-8523000	Active TSS	Brain Angular Gyrus	brain
30	chr8:8522400-8523000	Flanking Active TSS	HMEC	breast
31	chr8:8522400-8523200	Active TSS	Fetal Brain Female	brain
32	chr8:8522400-8523400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr8:8522400-8523400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr8:8522400-8523600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:8522400-8525600	Weak transcription	Fetal Lung	lung
36	chr8:8522600-8523000	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr8:8522600-8523000	Active TSS	Brain Anterior Caudate	brain
38	chr8:8522600-8523000	Active TSS	Brain Germinal Matrix	brain
39	chr8:8522600-8523000	Active TSS	Brain Hippocampus Middle	brain
40	chr8:8522600-8523000	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr8:8522600-8523000	Active TSS	Brain Substantia Nigra	brain
42	chr8:8522600-8523000	Active TSS	HSMMtube	muscle
43	chr8:8522600-8523200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:8522600-8523200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:8522600-8527400	Enhancers	A549	lung
46	chr8:8522800-8523000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:8522800-8523000	Enhancers	HSMM	muscle
48	chr8:8522800-8523000	Enhancers	Osteobl	bone
49	chr8:8522800-8523200	Enhancers	Brain Cingulate Gyrus	brain
50	chr8:8522800-8523600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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