Variant report

Variant	esv34347
Chromosome Location	chr8:91101339-91179126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:244)
Chromatin interactive
region (count:78)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 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	chr8:91177147-91177182	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:91131371-91131596	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:91131335-91131588	K562	blood:	n/a	n/a
4	ARID3A	chr8:91177637-91178012	K562	blood:	n/a	n/a
5	ARID3A	chr8:91151183-91151514	K562	blood:	n/a	n/a
6	ATF1	chr8:91177393-91178071	K562	blood:	n/a	n/a
7	BACH1	chr8:91178587-91178653	K562	blood:	n/a	n/a
8	BACH1	chr8:91145605-91145882	K562	blood:	n/a	n/a
9	BHLHE40	chr8:91177719-91178162	K562	blood:	n/a	n/a
10	BHLHE40	chr8:91178731-91178776	K562	blood:	n/a	n/a
11	CBX3	chr8:91151149-91151549	K562	blood:	n/a	n/a
12	CBX3	chr8:91151143-91151574	HCT-116	colon:	n/a	n/a
13	CBX3	chr8:91151169-91151656	HCT-116	colon:	n/a	n/a
14	CBX3	chr8:91151119-91151592	K562	blood:	n/a	n/a
15	CBX3	chr8:91113155-91113503	K562	blood:	n/a	n/a
16	CBX3	chr8:91158557-91158864	K562	blood:	n/a	n/a
17	CBX3	chr8:91131223-91131598	HCT-116	colon:	n/a	n/a
18	CCNT2	chr8:91177757-91177993	K562	blood:	n/a	n/a
19	CEBPB	chr8:91166298-91166360	K562	blood:	n/a	n/a
20	CEBPB	chr8:91169303-91169578	A549	lung:	n/a	chr8:91169472-91169483
21	CEBPB	chr8:91169314-91169620	HepG2	liver:	n/a	chr8:91169472-91169483
22	CEBPB	chr8:91141017-91141077	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:91177767-91178085	K562	blood:	n/a	n/a
24	CEBPB	chr8:91104769-91104775	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:91114882-91115172	HepG2	liver:	n/a	chr8:91115061-91115072
26	CEBPB	chr8:91148312-91148337	K562	blood:	n/a	n/a
27	CEBPB	chr8:91114908-91115149	IMR90	lung:	n/a	chr8:91115061-91115072
28	CEBPB	chr8:91132810-91133055	K562	blood:	n/a	n/a
29	CEBPB	chr8:91169323-91169629	K562	blood:	n/a	chr8:91169472-91169483
30	CEBPB	chr8:91169328-91169642	H1-hESC	embryonic stem cell:	n/a	chr8:91169472-91169483
31	CEBPB	chr8:91131333-91131699	K562	blood:	n/a	n/a
32	CEBPB	chr8:91169336-91169634	IMR90	lung:	n/a	chr8:91169472-91169483
33	CEBPB	chr8:91114951-91115151	K562	blood:	n/a	chr8:91115061-91115072
34	CHD2	chr8:91178899-91179228	K562	blood:	n/a	n/a
35	CHD2	chr8:91122326-91122363	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr8:91127776-91127781	K562	blood:	n/a	n/a
37	CREB1	chr8:91115132-91115359	GM12878	blood:	n/a	n/a
38	CTCF	chr8:91131380-91131530	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr8:91131380-91131530	Caco-2	colon:	n/a	n/a
40	CTCF	chr8:91131620-91131770	GM12872	blood:	n/a	n/a
41	CTCF	chr8:91131360-91131510	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:91131360-91131510	HVMF	connective:	n/a	n/a
43	CTCF	chr8:91131360-91131510	RPTEC	kidney:	n/a	n/a
44	CTCF	chr8:91131380-91131530	BE2_C	brain:	n/a	n/a
45	CTCF	chr8:91168140-91168290	NHEK	skin:	n/a	n/a
46	CTCF	chr8:91131380-91131530	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr8:91131760-91131910	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr8:91143020-91143170	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:91131340-91131490	HAc	cerebellar:	n/a	n/a
50	CTCF	chr8:91131380-91131530	SAEC	small airway:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:91108188-91108238	AG09319	gingival:	n/a
2	chr8:91108620-91108670	HepG2	liver:	n/a
3	chr8:91173192-91173242	Caco-2	colon:	n/a
4	chr8:91108188-91108238	GM12891	blood:	n/a
5	chr8:91122625-91122675	Hela-S3	cervix:	n/a
6	chr8:91173192-91173242	PANC-1	pancreas:	n/a
7	chr8:91108188-91108238	IMR90	lung:	fetal
8	chr8:91108620-91108670	HCM	heart:	n/a
9	chr8:91122625-91122675	ECC-1	luminal epithelium:	n/a
10	chr8:91122625-91122675	NB4	blood:	n/a
11	chr8:91173192-91173242	NHDF-neo	bronchial:	n/a
12	chr8:91173192-91173242	AG04450	lung:	fetal
13	chr8:91108188-91108238	AoSMC	blood vessel:	n/a
14	chr8:91173192-91173242	GM06990	blood:	n/a
15	chr8:91108620-91108670	GM12892	blood:	n/a
16	chr8:91108188-91108238	CMK	blood:	n/a
17	chr8:91108188-91108238	AG04450	lung:	fetal
18	chr8:91108620-91108670	IMR90	lung:	fetal
19	chr8:91173192-91173242	GM12878	blood:	n/a
20	chr8:91122625-91122675	MCF10A-Er-Src	breast:	n/a
21	chr8:91108188-91108238	U87	brain:	n/a
22	chr8:91108188-91108238	RPTEC	kidney:	n/a
23	chr8:91122625-91122675	NHBE	bronchial:	n/a
24	chr8:91108188-91108238	PFSK-1	brain:	n/a
25	chr8:91108188-91108238	HMEC	breast:	n/a
26	chr8:91173192-91173242	ProgFib	skin:	n/a
27	chr8:91108620-91108670	AG10803	skin:	n/a
28	chr8:91108188-91108238	K562	blood:	n/a
29	chr8:91108620-91108670	GM12891	blood:	n/a
30	chr8:91173192-91173242	IMR90	lung:	fetal
31	chr8:91108620-91108670	NHDF-neo	bronchial:	n/a
32	chr8:91122625-91122675	HEEpiC	esophagus:	n/a
33	chr8:91173192-91173242	HRCEpiC	kidney:	n/a
34	chr8:91173192-91173242	ECC-1	luminal epithelium:	n/a
35	chr8:91108620-91108670	AG09319	gingival:	n/a
36	chr8:91122625-91122675	SK-N-SH_RA	brain:	n/a
37	chr8:91173192-91173242	HCF	heart:	n/a
38	chr8:91108620-91108670	K562	blood:	n/a
39	chr8:91122625-91122675	Caco-2	colon:	n/a
40	chr8:91108620-91108670	PANC-1	pancreas:	n/a
41	chr8:91122625-91122675	LNCaP	prostate:	n/a
42	chr8:91108188-91108238	HCF	heart:	n/a
43	chr8:91122625-91122675	SK-N-SH	brain:	n/a
44	chr8:91122625-91122675	HRCEpiC	kidney:	n/a
45	chr8:91108620-91108670	HMEC	breast:	n/a
46	chr8:91108620-91108670	NHBE	bronchial:	n/a
47	chr8:91108620-91108670	T-47D	breast:	n/a
48	chr8:91108620-91108670	GM19239	blood:	n/a
49	chr8:91173192-91173242	AG04449	skin:	fetal
50	chr8:91108188-91108238	HAEpiC	amniotic membrane:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:91152815..91155655-chr8:91173130..91176716,3	K562	blood:
2	chr8:91132201..91135779-chr8:91136191..91140111,5	K562	blood:
3	chr11:62608625..62609221-chr8:91155315..91155835,7	Hela-S3	cervix:
4	chr8:91124236..91126354-chr8:91127708..91130462,3	K562	blood:
5	chr8:91147559..91149333-chr8:91149413..91151498,3	K562	blood:
6	chr11:62608628..62609154-chr8:91155316..91155836,3	MCF-7	breast:
7	chr17:41465192..41465706-chr8:91155316..91155835,2	HCT-116	colon:
8	chr1:245027270..245028019-chr8:91135650..91136189,2	MCF-7	breast:
9	chr8:91155035..91157497-chr8:91163156..91166027,2	K562	blood:
10	chr17:41463347..41467815-chr8:91153835..91156835,9	K562	blood:
11	chr8:91147559..91149333-chr8:91149413..91151498,3	K562	blood:
12	chr8:91134530..91136835-chr8:91178960..91180753,2	K562	blood:
13	chr3:73159952..73160589-chr8:91154816..91155815,2	Hela-S3	cervix:
14	chr11:62608623..62609195-chr8:91155314..91155835,10	HCT-116	colon:
15	chr8:91110151..91112011-chr8:91117979..91120218,2	K562	blood:
16	chr8:91175219..91178633-chr8:91184019..91187268,3	K562	blood:
17	chr8:91148105..91150746-chr8:91155344..91157015,2	K562	blood:
18	chr17:41398631..41400267-chr8:91153816..91155335,2	K562	blood:
19	chr8:91166036..91168487-chr8:91169692..91172196,2	MCF-7	breast:
20	chr4:6564574..6566094-chr8:91155316..91156835,2	K562	blood:
21	chr8:91139396..91140972-chr8:91161545..91163760,2	K562	blood:
22	chr11:62608628..62609148-chr8:91155315..91155836,4	NB4	blood:
23	chr8:91177407..91179281-chr8:91196128..91199121,2	MCF-7	breast:
24	chr8:91126270..91128899-chr8:91135979..91138410,2	K562	blood:
25	chr8:91177720..91183484-chr8:91189779..91192790,4	K562	blood:
26	chr8:91160123..91162835-chr8:91174934..91176685,2	K562	blood:
27	chr8:91092897..91095397-chr8:91099326..91102045,2	K562	blood:
28	chr8:91143386..91146044-chr8:91149940..91153117,3	K562	blood:
29	chr8:91155035..91157497-chr8:91163156..91166027,2	K562	blood:
30	chr10:103124108..103124630-chr8:91155315..91155836,3	HCT-116	colon:
31	chr8:91143386..91146044-chr8:91149940..91153117,3	K562	blood:
32	chr8:91142074..91143853-chr8:91145432..91147703,2	K562	blood:
33	chr1:160080964..160082487-chr8:91155315..91156836,2	K562	blood:
34	chr8:91139396..91140972-chr8:91161545..91163760,2	K562	blood:
35	chr8:91126270..91128899-chr8:91135979..91138410,2	K562	blood:
36	chr17:41400577..41402205-chr8:91155335..91156836,2	K562	blood:
37	chr8:91111364..91113093-chr8:91113728..91115750,2	K562	blood:
38	chr8:91142074..91143853-chr8:91145432..91147703,2	K562	blood:
39	chr8:91013417..91015072-chr8:91160846..91162367,2	MCF-7	breast:
40	chr8:91152701..91155166-chr8:91157223..91159554,2	K562	blood:
41	chr8:91152815..91155655-chr8:91173130..91176716,3	K562	blood:
42	chr17:41463347..41467581-chr8:91153836..91156836,7	K562	blood:
43	chr8:91109881..91112864-chr8:91114233..91115750,2	K562	blood:
44	chr8:91148105..91150746-chr8:91155344..91157015,2	K562	blood:
45	chr8:91143606..91145604-chr8:91237948..91239469,2	K562	blood:
46	chr8:91177486..91179176-chr8:91180628..91182984,2	K562	blood:
47	chr8:91152980..91155385-chr8:91174154..91176618,2	K562	blood:
48	chr3:73158464..73161607-chr8:91155315..91156835,5	K562	blood:
49	chr8:91121306..91123004-chr8:91234013..91235686,2	K562	blood:
50	chr8:90791149..90792881-chr8:91130629..91132427,2	K562	blood:

No data

Variant related genes	Relation type
CALB1	TF binding region
CALB1	CpG island
ENSG00000104320	chromatin interactions
ENSG00000153187	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000074211	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000104327	chromatin interactions

Extended variants
information (count: 2204 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2204 , 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	rs12549107	chr8:91101339-91101340	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543345660	chr8:91101403-91101404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12541460	chr8:91101409-91101410	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533154973	chr8:91101420-91101421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112191358	chr8:91101428-91101429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368424885	chr8:91101471-91101472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111732199	chr8:91101484-91101485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73694307	chr8:91101499-91101500	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10104321	chr8:91101529-91101530	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs549073239	chr8:91101541-91101542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375354948	chr8:91101542-91101543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567748978	chr8:91101555-91101556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149988401	chr8:91101559-91101560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550185843	chr8:91101618-91101619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145227517	chr8:91101670-91101671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188299485	chr8:91101686-91101687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77059581	chr8:91101718-91101719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569247595	chr8:91101735-91101736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572073906	chr8:91101744-91101745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536313492	chr8:91101745-91101746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369941852	chr8:91101795-91101796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576157007	chr8:91101829-91101830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543632625	chr8:91101854-91101855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148742056	chr8:91101861-91101862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577036948	chr8:91101872-91101873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs34915823	chr8:91101879-91101880	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs560072950	chr8:91101887-91101888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527718554	chr8:91101912-91101913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs78397930	chr8:91101929-91101930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75364940	chr8:91101932-91101933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561460729	chr8:91101939-91101940	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531797457	chr8:91101950-91101951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs550314878	chr8:91102018-91102019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571771034	chr8:91102036-91102037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146840961	chr8:91102086-91102087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58769148	chr8:91102107-91102108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs193290166	chr8:91102163-91102164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536302995	chr8:91102170-91102171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555672696	chr8:91102184-91102185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34243721	chr8:91102212-91102213	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569696420	chr8:91102227-91102228	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536766573	chr8:91102252-91102253	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140683401	chr8:91102277-91102278	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576971757	chr8:91102304-91102305	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575942618	chr8:91102312-91102313	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373334230	chr8:91102344-91102345	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540915995	chr8:91102351-91102352	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552894512	chr8:91102355-91102356	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555137293	chr8:91102377-91102378	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572085840	chr8:91102378-91102379	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91100600-91102200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:91100600-91102400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr8:91102200-91102600	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr8:91102400-91102600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr8:91102600-91104600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:91104200-91105800	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr8:91104600-91105000	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr8:91105000-91105600	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
9	chr8:91105600-91107000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:91105800-91106600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:91106600-91108200	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr8:91107000-91107400	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr8:91107400-91108200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:91108200-91108400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr8:91110000-91114000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:91121800-91122000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:91121800-91122200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:91121800-91122600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr8:91122000-91122400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:91122000-91122400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr8:91122200-91123400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr8:91122200-91123800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr8:91122400-91123600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:91122600-91128200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:91123400-91124400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:91123600-91124200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:91123600-91124600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:91123600-91124600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:91123800-91124600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:91124200-91124600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr8:91124200-91126800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:91124400-91127400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr8:91124600-91124800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr8:91124600-91125000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr8:91124600-91127600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr8:91124600-91128000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr8:91124800-91128200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:91126800-91127000	Enhancers	Esophagus	oesophagus
39	chr8:91126800-91127000	ZNF genes & repeats	Pancreas	Pancrea
40	chr8:91126800-91127200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:91127200-91130200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:91127400-91127600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr8:91127600-91128000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr8:91127600-91128000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:91127600-91128400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:91127600-91128800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:91128000-91128400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:91128000-91128600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:91128000-91128600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr8:91128200-91128800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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