Variant report

Variant	nsv1022784
Chromosome Location	chr8:8271462-8309864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

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	ATF3	chr8:8286690-8287352	A549	lung:	n/a	n/a
6	ATF3	chr8:8286695-8287347	A549	lung:	n/a	n/a
7	BCL3	chr8:8286570-8287287	A549	lung:	n/a	n/a
8	BCL3	chr8:8286658-8287363	A549	lung:	n/a	n/a
9	BHLHE40	chr8:8285152-8285676	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
10	BHLHE40	chr8:8286354-8287280	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:8285206-8285429	K562	blood:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
12	BHLHE40	chr8:8285203-8285486	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
13	BHLHE40	chr8:8284870-8286026	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
14	BRCA1	chr8:8274625-8275040	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:8283400-8283413	HepG2	liver:	n/a	n/a
16	CBX3	chr8:8293023-8293525	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:8298711-8299537	HCT-116	colon:	n/a	n/a
18	CBX3	chr8:8293104-8293495	K562	blood:	n/a	n/a
19	CBX3	chr8:8293081-8293537	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:8298667-8299528	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:8293131-8293493	K562	blood:	n/a	n/a
22	CEBPB	chr8:8286999-8287221	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:8286731-8287340	A549	lung:	n/a	n/a
24	CEBPB	chr8:8307022-8307239	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:8286803-8287335	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:8309492-8309730	IMR90	lung:	n/a	chr8:8309599-8309610
27	CEBPB	chr8:8288159-8288360	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr8:8286926-8287259	A549	lung:	n/a	n/a
29	CEBPB	chr8:8309555-8309742	HepG2	liver:	n/a	chr8:8309599-8309610
30	CEBPB	chr8:8306900-8307304	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:8286874-8287324	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:8286862-8287314	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:8277590-8277799	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:8309467-8309731	A549	lung:	n/a	chr8:8309599-8309610
35	CEBPB	chr8:8305274-8305363	A549	lung:	n/a	n/a
36	CEBPB	chr8:8285267-8285739	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:8274608-8275045	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:8286904-8287289	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:8286630-8287443	A549	lung:	n/a	n/a
40	CEBPD	chr8:8286992-8287221	HepG2	liver:	n/a	n/a
41	CEBPD	chr8:8286964-8287209	HepG2	liver:	n/a	n/a
42	CHD2	chr8:8286860-8287226	HepG2	liver:	n/a	n/a
43	CREB1	chr8:8286512-8287343	HepG2	liver:	n/a	n/a
44	CTCF	chr8:8294840-8294890	GM13976	blood:	n/a	n/a
45	CTCF	chr8:8283262-8283352	K562	blood:	n/a	n/a
46	CTCF	chr8:8308183-8308224	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr8:8283188-8283419	K562	blood:	n/a	n/a
48	CTCF	chr8:8300220-8300370	SAEC	small airway:	n/a	n/a
49	CTCF	chr8:8281308-8281347	NHEK	skin:	n/a	n/a
50	CTCF	chr8:8281270-8281355	Pancreas_OC	pancreas:	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	CMK	blood:	n/a
2	chr8:8283032-8283082	K562	blood:	n/a
3	chr8:8283032-8283082	PANC-1	pancreas:	n/a
4	chr8:8283032-8283082	H1-hESC	embryonic stem cell:	embryo
5	chr8:8283032-8283082	SK-N-MC	brain:	n/a
6	chr8:8283032-8283082	HCPEpiC	choroid plexus:	n/a
7	chr8:8283032-8283082	HepG2	liver:	n/a
8	chr8:8283032-8283082	HCF	heart:	n/a
9	chr8:8283032-8283082	SKMC	muscle:	n/a
10	chr8:8283032-8283082	GM12878	blood:	n/a
11	chr8:8283032-8283082	U87	brain:	n/a
12	chr8:8283032-8283082	PFSK-1	brain:	n/a
13	chr8:8283032-8283082	HRPEpiC	eye:	n/a
14	chr8:8283032-8283082	Jurkat	blood:	n/a
15	chr8:8283032-8283082	HCM	heart:	n/a
16	chr8:8283032-8283082	AG09309	skin:	n/a
17	chr8:8283032-8283082	SAEC	small airway:	n/a
18	chr8:8283032-8283082	HEK293	kidney:	embryo
19	chr8:8283032-8283082	RPTEC	kidney:	n/a
20	chr8:8283032-8283082	LNCaP	prostate:	n/a
21	chr8:8283032-8283082	HCT-116	colon:	n/a
22	chr8:8283032-8283082	ovcar-3	ovarian:	n/a
23	chr8:8283032-8283082	SK-N-SH_RA	brain:	n/a
24	chr8:8283032-8283082	Hepatocyte	liver:	n/a
25	chr8:8283032-8283082	AG04450	lung:	fetal
26	chr8:8283032-8283082	HUVEC	blood vessel:	n/a
27	chr8:8283032-8283082	HRCEpiC	kidney:	n/a
28	chr8:8283032-8283082	AG10803	skin:	n/a
29	chr8:8283032-8283082	PrEC	prostate:	n/a
30	chr8:8283032-8283082	NH-A	brain:	n/a
31	chr8:8283032-8283082	AG04449	skin:	fetal
32	chr8:8283032-8283082	A549	lung:	n/a
33	chr8:8283032-8283082	HEEpiC	esophagus:	n/a
34	chr8:8283032-8283082	NT2-D1	testis:	n/a
35	chr8:8283032-8283082	ProgFib	skin:	n/a
36	chr8:8283032-8283082	HAEpiC	amniotic membrane:	n/a
37	chr8:8283032-8283082	T-47D	breast:	n/a
38	chr8:8283032-8283082	HRE	kidney:	n/a
39	chr8:8283032-8283082	NB4	blood:	n/a
40	chr8:8283032-8283082	GM12892	blood:	n/a
41	chr8:8283032-8283082	HL-60	blood:	n/a
42	chr8:8283032-8283082	Caco-2	colon:	n/a
43	chr8:8283032-8283082	MCF10A-Er-Src	breast:	n/a
44	chr8:8283032-8283082	NHBE	bronchial:	n/a
45	chr8:8283032-8283082	SK-N-SH	brain:	n/a
46	chr8:8283032-8283082	HMEC	breast:	n/a
47	chr8:8283032-8283082	AG09319	gingival:	n/a
48	chr8:8283032-8283082	IMR90	lung:	fetal
49	chr8:8283032-8283082	Hela-S3	cervix:	n/a
50	chr8:8283032-8283082	GM19239	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8307087..8309406-chr8:8317216..8320167,2	MCF-7	breast:
2	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
3	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
4	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
5	chr8:8299017..8300539-chr8:8317523..8321166,3	MCF-7	breast:
6	chr8:8243810..8245986-chr8:8307375..8310131,2	MCF-7	breast:
7	chr8:8239788..8242444-chr8:8287010..8288532,2	MCF-7	breast:
8	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
9	chr8:8301355..8304096-chr8:8318371..8320187,2	MCF-7	breast:
10	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
11	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
12	chr8:8242445..8245313-chr8:8297878..8301672,4	MCF-7	breast:
13	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
14	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
15	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
16	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
17	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
18	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
19	chr8:8242907..8245706-chr8:8295976..8300172,6	MCF-7	breast:
20	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
21	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
22	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
23	chr8:8306469..8311532-chr8:8316315..8320180,6	MCF-7	breast:
24	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
25	chr8:8243706..8245938-chr8:8270141..8271973,2	MCF-7	breast:
26	chr8:8151768..8153956-chr8:8305542..8308270,3	MCF-7	breast:
27	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
28	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
29	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
30	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
31	chr8:8281489..8283205-chr8:8283537..8285806,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-1	chr8:8281998-8282142	ENSG00000253505
2	lnc-PRAGMIN.1-1	chr8:8281998-8282088	ENSG00000253505
3	lnc-PRAGMIN.1-1	chr8:8279934-8280523	ENSG00000253505
4	lnc-PRAGMIN.1-1	chr8:8272200-8272611	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: 2190 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:2190 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551873250	chr8:8271502-8271503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568865072	chr8:8271510-8271511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538155381	chr8:8271521-8271522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371891926	chr8:8271525-8271526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548371517	chr8:8271554-8271555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368425752	chr8:8271556-8271557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548513745	chr8:8271566-8271567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148808453	chr8:8271571-8271572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534080759	chr8:8271592-8271593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537193398	chr8:8271593-8271594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570841656	chr8:8271594-8271595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556759343	chr8:8271613-8271614	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377419455	chr8:8271662-8271663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186599416	chr8:8271672-8271673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144884055	chr8:8271676-8271677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576421895	chr8:8271691-8271692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10092809	chr8:8271710-8271711	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147930653	chr8:8271744-8271745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574803115	chr8:8271764-8271765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540397730	chr8:8271778-8271779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560332809	chr8:8271780-8271781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533134583	chr8:8271787-8271788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532089872	chr8:8271802-8271803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190998924	chr8:8271806-8271807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562336591	chr8:8271811-8271812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531168863	chr8:8271813-8271814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115309604	chr8:8271826-8271827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183763514	chr8:8271830-8271831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs17669947	chr8:8271878-8271879	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs13265658	chr8:8271881-8271882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547562225	chr8:8271900-8271901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571071500	chr8:8271906-8271907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188309750	chr8:8271909-8271910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116492143	chr8:8271947-8271948	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141722174	chr8:8271951-8271952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147066190	chr8:8271971-8271972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs151071657	chr8:8271998-8271999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552521865	chr8:8272026-8272027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574772158	chr8:8272052-8272053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540564285	chr8:8272062-8272063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553683493	chr8:8272114-8272115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376711223	chr8:8272167-8272168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371331366	chr8:8272173-8272174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140977215	chr8:8272211-8272212	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs150204878	chr8:8272217-8272218	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs573212493	chr8:8272256-8272257	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs562557873	chr8:8272267-8272268	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs548613730	chr8:8272272-8272273	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs541390379	chr8:8272281-8272282	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs192615057	chr8:8272352-8272353	Weak transcription Enhancers	lncRNA	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:468 , 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	chr8:8269800-8272200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:8269800-8273800	Weak transcription	Hela-S3	cervix
5	chr8:8269800-8274000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:8269800-8274400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:8269800-8274600	Weak transcription	NHEK	skin
8	chr8:8270000-8274200	Weak transcription	Fetal Intestine Large	intestine
9	chr8:8270000-8284200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:8270800-8274000	Weak transcription	Fetal Intestine Small	intestine
11	chr8:8270800-8274800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr8:8271400-8274800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:8272200-8272600	Enhancers	Brain Cingulate Gyrus	brain
14	chr8:8272200-8272600	Enhancers	Brain Hippocampus Middle	brain
15	chr8:8272200-8273200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:8272400-8272600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:8272400-8272600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr8:8272400-8272800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:8272400-8275000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:8272600-8276200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr8:8272600-8276400	Weak transcription	Brain Hippocampus Middle	brain
22	chr8:8272800-8274800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:8273200-8289400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:8273600-8277200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr8:8273600-8281000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr8:8273800-8274000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:8273800-8274800	Enhancers	A549	lung
28	chr8:8273800-8275400	Enhancers	Hela-S3	cervix
29	chr8:8274000-8274400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:8274000-8276200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:8274000-8278200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:8274000-8282400	Enhancers	Fetal Intestine Small	intestine
33	chr8:8274200-8274800	Enhancers	Fetal Intestine Large	intestine
34	chr8:8274200-8275000	Enhancers	Fetal Lung	lung
35	chr8:8274400-8274600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:8274400-8276000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:8274600-8274800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:8274600-8276000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:8274600-8276000	Enhancers	NHEK	skin
40	chr8:8274600-8276800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:8274600-8277200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:8274600-8277800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr8:8274800-8275000	Enhancers	Brain Germinal Matrix	brain
44	chr8:8274800-8275200	Enhancers	Fetal Brain Male	brain
45	chr8:8274800-8275200	Enhancers	Fetal Heart	heart
46	chr8:8274800-8275400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:8274800-8275400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr8:8274800-8275400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr8:8274800-8275400	Flanking Active TSS	A549	lung
50	chr8:8274800-8276000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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