Variant report

Variant	nsv465451
Chromosome Location	chr8:8273043-8311298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:432)
CpG islands
(count:61)
Chromatin interactive
region (count:35)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8285133-8285725	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8286275-8287368	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8283141-8283395	HepG2	liver:	n/a	n/a
4	ATF2	chr8:8293199-8293483	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:8310031-8310713	GM12878	blood:	n/a	n/a
6	ATF2	chr8:8310015-8310665	GM12878	blood:	n/a	n/a
7	ATF3	chr8:8286695-8287347	A549	lung:	n/a	n/a
8	ATF3	chr8:8286690-8287352	A549	lung:	n/a	n/a
9	BATF	chr8:8310182-8310550	GM12878	blood:	n/a	n/a
10	BATF	chr8:8310225-8310548	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:8310128-8310497	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:8310249-8310487	GM12878	blood:	n/a	n/a
13	BCL3	chr8:8286570-8287287	A549	lung:	n/a	n/a
14	BCL3	chr8:8286658-8287363	A549	lung:	n/a	n/a
15	BCLAF1	chr8:8310124-8310538	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:8310038-8310609	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:8285206-8285429	K562	blood:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
18	BHLHE40	chr8:8284870-8286026	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
19	BHLHE40	chr8:8310177-8310477	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:8285203-8285486	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
21	BHLHE40	chr8:8285152-8285676	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
22	BHLHE40	chr8:8286354-8287280	HepG2	liver:	n/a	n/a
23	BRCA1	chr8:8283400-8283413	HepG2	liver:	n/a	n/a
24	BRCA1	chr8:8274625-8275040	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr8:8298711-8299537	HCT-116	colon:	n/a	n/a
26	CBX3	chr8:8298667-8299528	HCT-116	colon:	n/a	n/a
27	CBX3	chr8:8293104-8293495	K562	blood:	n/a	n/a
28	CBX3	chr8:8293023-8293525	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:8293131-8293493	K562	blood:	n/a	n/a
30	CBX3	chr8:8293081-8293537	HCT-116	colon:	n/a	n/a
31	CEBPB	chr8:8286904-8287289	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:8288159-8288360	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:8286630-8287443	A549	lung:	n/a	n/a
34	CEBPB	chr8:8307022-8307239	MCF-7	breast:	n/a	n/a
35	CEBPB	chr8:8305274-8305363	A549	lung:	n/a	n/a
36	CEBPB	chr8:8309492-8309730	IMR90	lung:	n/a	chr8:8309599-8309610
37	CEBPB	chr8:8309467-8309731	A549	lung:	n/a	chr8:8309599-8309610
38	CEBPB	chr8:8286999-8287221	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:8277590-8277799	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:8286803-8287335	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:8309555-8309742	HepG2	liver:	n/a	chr8:8309599-8309610
42	CEBPB	chr8:8286862-8287314	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:8274608-8275045	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr8:8286874-8287324	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:8286926-8287259	A549	lung:	n/a	n/a
46	CEBPB	chr8:8286731-8287340	A549	lung:	n/a	n/a
47	CEBPB	chr8:8306900-8307304	MCF-7	breast:	n/a	n/a
48	CEBPB	chr8:8285267-8285739	HepG2	liver:	n/a	n/a
49	CEBPD	chr8:8286964-8287209	HepG2	liver:	n/a	n/a
50	CEBPD	chr8:8286992-8287221	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8283032-8283082	SK-N-SH	brain:	n/a
2	chr8:8283032-8283082	HAEpiC	amniotic membrane:	n/a
3	chr8:8283032-8283082	Caco-2	colon:	n/a
4	chr8:8283032-8283082	AG09319	gingival:	n/a
5	chr8:8283032-8283082	GM12891	blood:	n/a
6	chr8:8283032-8283082	HRE	kidney:	n/a
7	chr8:8283032-8283082	ECC-1	luminal epithelium:	n/a
8	chr8:8283032-8283082	CMK	blood:	n/a
9	chr8:8283032-8283082	AG04450	lung:	fetal
10	chr8:8283032-8283082	HRPEpiC	eye:	n/a
11	chr8:8283032-8283082	PFSK-1	brain:	n/a
12	chr8:8283032-8283082	HEEpiC	esophagus:	n/a
13	chr8:8283032-8283082	T-47D	breast:	n/a
14	chr8:8283032-8283082	H1-hESC	embryonic stem cell:	embryo
15	chr8:8283032-8283082	Hela-S3	cervix:	n/a
16	chr8:8283032-8283082	AG10803	skin:	n/a
17	chr8:8283032-8283082	HCM	heart:	n/a
18	chr8:8283032-8283082	SAEC	small airway:	n/a
19	chr8:8283032-8283082	NHDF-neo	bronchial:	n/a
20	chr8:8283032-8283082	ProgFib	skin:	n/a
21	chr8:8283032-8283082	HUVEC	blood vessel:	n/a
22	chr8:8283032-8283082	HRCEpiC	kidney:	n/a
23	chr8:8283032-8283082	GM12878	blood:	n/a
24	chr8:8283032-8283082	K562	blood:	n/a
25	chr8:8283032-8283082	HEK293	kidney:	embryo
26	chr8:8283032-8283082	NB4	blood:	n/a
27	chr8:8283032-8283082	AoSMC	blood vessel:	n/a
28	chr8:8283032-8283082	LNCaP	prostate:	n/a
29	chr8:8283032-8283082	IMR90	lung:	fetal
30	chr8:8283032-8283082	HIPEpiC	eye:	n/a
31	chr8:8283032-8283082	SK-N-MC	brain:	n/a
32	chr8:8283032-8283082	HCF	heart:	n/a
33	chr8:8283032-8283082	AG09309	skin:	n/a
34	chr8:8283032-8283082	BJ	skin:	n/a
35	chr8:8283032-8283082	SK-N-SH_RA	brain:	n/a
36	chr8:8283032-8283082	MCF-7	breast:	n/a
37	chr8:8283032-8283082	GM06990	blood:	n/a
38	chr8:8283032-8283082	ovcar-3	ovarian:	n/a
39	chr8:8283032-8283082	NH-A	brain:	n/a
40	chr8:8283032-8283082	NT2-D1	testis:	n/a
41	chr8:8283032-8283082	HNPCEpiC	eye:	n/a
42	chr8:8283032-8283082	MCF10A-Er-Src	breast:	n/a
43	chr8:8283032-8283082	A549	lung:	n/a
44	chr8:8283032-8283082	BE2_C	brain:	n/a
45	chr8:8283032-8283082	RPTEC	kidney:	n/a
46	chr8:8283032-8283082	AG04449	skin:	fetal
47	chr8:8283032-8283082	Jurkat	blood:	n/a
48	chr8:8283032-8283082	HL-60	blood:	n/a
49	chr8:8283032-8283082	HepG2	liver:	n/a
50	chr8:8283032-8283082	HPAEpiC	pulmonary alveolar:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
2	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
3	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
4	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
5	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
6	chr8:8151768..8153956-chr8:8305542..8308270,3	MCF-7	breast:
7	chr8:8237866..8240823-chr8:8310722..8313327,2	MCF-7	breast:
8	chr8:8241777..8245267-chr8:8311182..8314962,7	MCF-7	breast:
9	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
10	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:
11	chr8:8306469..8311532-chr8:8316315..8320180,6	MCF-7	breast:
12	chr8:8307087..8309406-chr8:8317216..8320167,2	MCF-7	breast:
13	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
14	chr8:8281489..8283205-chr8:8283537..8285806,2	MCF-7	breast:
15	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
16	chr8:8301355..8304096-chr8:8318371..8320187,2	MCF-7	breast:
17	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
18	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
19	chr8:8239788..8242444-chr8:8287010..8288532,2	MCF-7	breast:
20	chr8:8242907..8245706-chr8:8295976..8300172,6	MCF-7	breast:
21	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
22	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
23	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
24	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
25	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
26	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
27	chr8:8243810..8245986-chr8:8307375..8310131,2	MCF-7	breast:
28	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
29	chr8:8299017..8300539-chr8:8317523..8321166,3	MCF-7	breast:
30	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
31	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
32	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
33	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
34	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
35	chr8:8242445..8245313-chr8:8297878..8301672,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-1	chr8:8281998-8282088	ENSG00000253505
2	lnc-PRAGMIN.1-1	chr8:8281998-8282142	ENSG00000253505
3	lnc-PRAGMIN.1-1	chr8:8279934-8280523	ENSG00000253505

No data

Variant related genes	Relation type
ENSG00000253505	TF binding region
ENSG00000253505	CpG island
ENSG00000253505	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions

Extended variants
information (count: 2202 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:2202 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1971412	chr8:8273043-8273044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560480001	chr8:8273076-8273077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73525467	chr8:8273085-8273086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534972275	chr8:8273090-8273091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551507097	chr8:8273114-8273115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189922661	chr8:8273132-8273133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539386467	chr8:8273146-8273147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148650440	chr8:8273158-8273159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75210134	chr8:8273180-8273181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs58836411	chr8:8273181-8273182	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs116895214	chr8:8273190-8273191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535190117	chr8:8273212-8273213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117413027	chr8:8273217-8273218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540984668	chr8:8273243-8273244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199942743	chr8:8273272-8273273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201212333	chr8:8273274-8273275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563958318	chr8:8273280-8273281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578182749	chr8:8273281-8273282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199738543	chr8:8273282-8273283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543810497	chr8:8273283-8273284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200086108	chr8:8273286-8273287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs66685552	chr8:8273287-8273288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529471847	chr8:8273299-8273300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549602894	chr8:8273328-8273329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192575078	chr8:8273339-8273340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185434251	chr8:8273342-8273343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530603303	chr8:8273352-8273353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1543186	chr8:8273358-8273359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs571598052	chr8:8273360-8273361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533246002	chr8:8273366-8273367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549622520	chr8:8273382-8273383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569617231	chr8:8273390-8273391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1971411	chr8:8273407-8273408	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs555157380	chr8:8273424-8273425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565749983	chr8:8273425-8273426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534444764	chr8:8273430-8273431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150721480	chr8:8273440-8273441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577610142	chr8:8273458-8273459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6989256	chr8:8273497-8273498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557642607	chr8:8273516-8273517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62498668	chr8:8273519-8273520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564424212	chr8:8273520-8273521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543210395	chr8:8273548-8273549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560022480	chr8:8273559-8273560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189911049	chr8:8273594-8273595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545211147	chr8:8273595-8273596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565389017	chr8:8273620-8273621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530763988	chr8:8273665-8273666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144946626	chr8:8273688-8273689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569577940	chr8:8273714-8273715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8266600-8274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:8269600-8273800	Weak transcription	A549	lung
3	chr8:8269800-8273800	Weak transcription	Hela-S3	cervix
4	chr8:8269800-8274000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:8269800-8274400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:8269800-8274600	Weak transcription	NHEK	skin
7	chr8:8270000-8274200	Weak transcription	Fetal Intestine Large	intestine
8	chr8:8270000-8284200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:8270800-8274000	Weak transcription	Fetal Intestine Small	intestine
10	chr8:8270800-8274800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:8271400-8274800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr8:8272200-8273200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:8272400-8275000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:8272600-8276200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr8:8272600-8276400	Weak transcription	Brain Hippocampus Middle	brain
16	chr8:8272800-8274800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr8:8273200-8289400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:8273600-8277200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:8273600-8281000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:8273800-8274000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:8273800-8274800	Enhancers	A549	lung
22	chr8:8273800-8275400	Enhancers	Hela-S3	cervix
23	chr8:8274000-8274400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:8274000-8276200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:8274000-8278200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:8274000-8282400	Enhancers	Fetal Intestine Small	intestine
27	chr8:8274200-8274800	Enhancers	Fetal Intestine Large	intestine
28	chr8:8274200-8275000	Enhancers	Fetal Lung	lung
29	chr8:8274400-8274600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:8274400-8276000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:8274600-8274800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:8274600-8276000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:8274600-8276000	Enhancers	NHEK	skin
34	chr8:8274600-8276800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr8:8274600-8277200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr8:8274600-8277800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr8:8274800-8275000	Enhancers	Brain Germinal Matrix	brain
38	chr8:8274800-8275200	Enhancers	Fetal Brain Male	brain
39	chr8:8274800-8275200	Enhancers	Fetal Heart	heart
40	chr8:8274800-8275400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr8:8274800-8275400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr8:8274800-8275400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr8:8274800-8275400	Flanking Active TSS	A549	lung
44	chr8:8274800-8276000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:8274800-8276000	Enhancers	Duodenum Mucosa	Duodenum
46	chr8:8274800-8276000	Weak transcription	Fetal Intestine Large	intestine
47	chr8:8274800-8276200	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:8274800-8276400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr8:8274800-8277200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr8:8274800-8277600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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