Variant report

Variant	nsv879021
Chromosome Location	chr4:56482750-56648713
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1367)
CpG islands
(count:1346)
Chromatin interactive
region (count:115)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56503388-56504015	K562	blood:	n/a	n/a
2	ARID3A	chr4:56493426-56493494	K562	blood:	n/a	n/a
3	ARID3A	chr4:56602788-56603227	K562	blood:	n/a	n/a
4	ARID3A	chr4:56589584-56589800	K562	blood:	n/a	n/a
5	ARID3A	chr4:56501495-56501827	K562	blood:	n/a	n/a
6	ARID3A	chr4:56536930-56537271	K562	blood:	n/a	n/a
7	ARID3A	chr4:56535243-56535280	K562	blood:	n/a	n/a
8	ARID3A	chr4:56599903-56600328	K562	blood:	n/a	n/a
9	ARID3A	chr4:56518503-56518691	K562	blood:	n/a	n/a
10	ARID3A	chr4:56595714-56597053	K562	blood:	n/a	n/a
11	ARID3A	chr4:56602821-56603153	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:56602401-56602562	K562	blood:	n/a	n/a
13	ARID3A	chr4:56515038-56515098	K562	blood:	n/a	n/a
14	ARID3A	chr4:56608965-56609070	K562	blood:	n/a	n/a
15	ARID3A	chr4:56597276-56597725	K562	blood:	n/a	n/a
16	ARID3A	chr4:56519920-56520587	K562	blood:	n/a	n/a
17	ATF1	chr4:56501416-56501837	K562	blood:	n/a	n/a
18	ATF1	chr4:56595957-56597096	K562	blood:	n/a	n/a
19	ATF1	chr4:56536954-56537234	K562	blood:	n/a	n/a
20	ATF1	chr4:56498147-56498454	K562	blood:	n/a	n/a
21	ATF3	chr4:56634460-56634806	K562	blood:	n/a	n/a
22	ATF3	chr4:56599950-56600410	K562	blood:	n/a	n/a
23	ATF3	chr4:56600082-56600281	K562	blood:	n/a	n/a
24	BACH1	chr4:56503593-56503801	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:56483945-56484132	K562	blood:	n/a	n/a
26	BACH1	chr4:56539608-56539938	K562	blood:	n/a	n/a
27	BACH1	chr4:56502324-56502563	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr4:56502806-56503160	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:56503675-56503978	K562	blood:	n/a	n/a
30	BACH1	chr4:56539736-56539823	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:56608951-56609115	K562	blood:	n/a	n/a
32	BATF	chr4:56483976-56484328	GM12878	blood:	n/a	n/a
33	BATF	chr4:56483933-56484337	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:56608920-56609395	K562	blood:	n/a	n/a
35	BHLHE40	chr4:56589634-56589918	K562	blood:	n/a	n/a
36	BHLHE40	chr4:56600069-56600344	K562	blood:	n/a	n/a
37	BHLHE40	chr4:56502266-56502629	K562	blood:	n/a	n/a
38	BHLHE40	chr4:56595973-56597056	K562	blood:	n/a	n/a
39	BHLHE40	chr4:56501226-56501818	K562	blood:	n/a	n/a
40	BHLHE40	chr4:56504145-56504547	K562	blood:	n/a	n/a
41	BHLHE40	chr4:56520557-56520573	K562	blood:	n/a	n/a
42	BHLHE40	chr4:56602362-56602445	K562	blood:	n/a	n/a
43	BRCA1	chr4:56620954-56621308	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr4:56537821-56538180	K562	blood:	n/a	n/a
45	CBX3	chr4:56537757-56538653	K562	blood:	n/a	n/a
46	CBX3	chr4:56595807-56596612	K562	blood:	n/a	n/a
47	CBX3	chr4:56547683-56548206	K562	blood:	n/a	n/a
48	CBX3	chr4:56599906-56600578	HCT-116	colon:	n/a	n/a
49	CBX3	chr4:56504056-56504491	K562	blood:	n/a	n/a
50	CCNT2	chr4:56595990-56597051	K562	blood:	n/a	n/a

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56501727-56501777	HRCEpiC	kidney:	n/a
2	chr4:56500362-56500412	RPTEC	kidney:	n/a
3	chr4:56499522-56499572	HCT-116	colon:	n/a
4	chr4:56501978-56502028	AG09319	gingival:	n/a
5	chr4:56501727-56501777	HRCEpiC	kidney:	n/a
6	chr4:56500362-56500412	RPTEC	kidney:	n/a
7	chr4:56499522-56499572	HCT-116	colon:	n/a
8	chr4:56501978-56502028	AG09319	gingival:	n/a
9	chr4:56501727-56501777	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:56502898-56502948	HAEpiC	amniotic membrane:	n/a
11	chr4:56534223-56534273	IMR90	lung:	fetal
12	chr4:56502116-56502166	GM06990	blood:	n/a
13	chr4:56502544-56502594	RPTEC	kidney:	n/a
14	chr4:56501727-56501777	SAEC	small airway:	n/a
15	chr4:56501978-56502028	GM06990	blood:	n/a
16	chr4:56501718-56501768	HRPEpiC	eye:	n/a
17	chr4:56534223-56534273	RPTEC	kidney:	n/a
18	chr4:56504657-56504707	IMR90	lung:	fetal
19	chr4:56502544-56502594	NHDF-neo	bronchial:	n/a
20	chr4:56496836-56496886	GM12892	blood:	n/a
21	chr4:56502664-56502714	ProgFib	skin:	n/a
22	chr4:56499522-56499572	CMK	blood:	n/a
23	chr4:56500362-56500412	GM06990	blood:	n/a
24	chr4:56504657-56504707	AG04449	skin:	fetal
25	chr4:56502469-56502519	K562	blood:	n/a
26	chr4:56502469-56502519	RPTEC	kidney:	n/a
27	chr4:56499522-56499572	HepG2	liver:	n/a
28	chr4:56501441-56501491	PANC-1	pancreas:	n/a
29	chr4:56502898-56502948	HCPEpiC	choroid plexus:	n/a
30	chr4:56502664-56502714	K562	blood:	n/a
31	chr4:56501441-56501491	H1-hESC	embryonic stem cell:	embryo
32	chr4:56500362-56500412	ovcar-3	ovarian:	n/a
33	chr4:56502544-56502594	HL-60	blood:	n/a
34	chr4:56502529-56502579	U87	brain:	n/a
35	chr4:56501441-56501491	Jurkat	blood:	n/a
36	chr4:56502864-56502914	HRPEpiC	eye:	n/a
37	chr4:56501727-56501777	NH-A	brain:	n/a
38	chr4:56502788-56502838	Caco-2	colon:	n/a
39	chr4:56502392-56502442	GM19239	blood:	n/a
40	chr4:56502529-56502579	NHBE	bronchial:	n/a
41	chr4:56502788-56502838	GM12878	blood:	n/a
42	chr4:56502116-56502166	NHDF-neo	bronchial:	n/a
43	chr4:56501978-56502028	NH-A	brain:	n/a
44	chr4:56502534-56502584	AG09309	skin:	n/a
45	chr4:56500362-56500412	HCM	heart:	n/a
46	chr4:56501441-56501491	CMK	blood:	n/a
47	chr4:56502116-56502166	GM12878	blood:	n/a
48	chr4:56502392-56502442	AG10803	skin:	n/a
49	chr4:56502864-56502914	SAEC	small airway:	n/a
50	chr4:56504657-56504707	ECC-1	luminal epithelium:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:56501844..56503895-chr4:56534983..56537847,2	K562	blood:
2	chr4:56571957..56574091-chr4:56598749..56600551,2	K562	blood:
3	chr4:56480747..56484464-chr4:56594012..56597947,4	K562	blood:
4	chr4:56517086..56520350-chr4:56522100..56524911,3	K562	blood:
5	chr4:56637771..56639865-chr4:56697633..56699417,2	MCF-7	breast:
6	chr4:56500691..56503425-chr4:56513263..56514979,2	K562	blood:
7	chr4:56588763..56591407-chr4:56594293..56596844,3	K562	blood:
8	chr4:56515936..56519934-chr4:56522100..56525314,4	K562	blood:
9	chr4:56529070..56532802-chr4:56534666..56538344,3	K562	blood:
10	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:
11	chr4:55837666..55838201-chr4:56602502..56603198,2	K562	blood:
12	chr4:56212321..56212921-chr4:56602569..56603071,2	K562	blood:
13	chr4:56632143..56634833-chr4:56645255..56648181,2	K562	blood:
14	chr4:56480747..56484464-chr4:56594012..56597947,4	K562	blood:
15	chr4:56520187..56522696-chr4:56535355..56536879,2	K562	blood:
16	chr4:56498450..56502811-chr4:56593362..56599516,6	K562	blood:
17	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
18	chr4:56212106..56214944-chr4:56536048..56538408,2	K562	blood:
19	chr4:56412329..56414161-chr4:56494486..56496762,2	K562	blood:
20	chr4:56522244..56525288-chr4:56525318..56527795,3	K562	blood:
21	chr4:56412086..56414460-chr4:56599995..56602256,4	MCF-7	breast:
22	chr4:56515936..56519934-chr4:56522100..56525314,4	K562	blood:
23	chr4:56567077..56569612-chr4:56570589..56573149,3	K562	blood:
24	chr4:56520187..56522696-chr4:56535355..56536879,2	K562	blood:
25	chr4:56571957..56574091-chr4:56598749..56600551,2	K562	blood:
26	chr4:56523921..56526378-chr4:56528208..56530318,2	K562	blood:
27	chr4:56550080..56552632-chr4:56586091..56588809,2	K562	blood:
28	chr4:56517086..56520350-chr4:56522100..56524911,3	K562	blood:
29	chr4:56520164..56522203-chr4:56529132..56532078,2	K562	blood:
30	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
31	chr4:56563632..56566026-chr4:56568439..56570285,2	K562	blood:
32	chr4:56407880..56411154-chr4:56599779..56601718,3	K562	blood:
33	chr4:56539528..56541945-chr4:56545482..56548185,2	K562	blood:
34	chr4:56503993..56504657-chr4:56601774..56602719,2	MCF-7	breast:
35	chr4:56408119..56414507-chr4:56501105..56505595,8	K562	blood:
36	chr4:56472523..56475869-chr4:56480434..56484043,4	K562	blood:
37	chr4:56609301..56611255-chr4:56614835..56616393,2	MCF-7	breast:
38	chr4:56567077..56569612-chr4:56570589..56573149,3	K562	blood:
39	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
40	chr4:56501908..56503959-chr4:56520105..56522203,2	K562	blood:
41	chr4:56613502..56615482-chr4:56616796..56619425,2	K562	blood:
42	chr4:56539528..56541945-chr4:56545482..56548185,2	K562	blood:
43	chr4:56481465..56483149-chr4:56595985..56597947,2	K562	blood:
44	chr4:56637542..56640482-chr4:56658130..56659977,2	K562	blood:
45	chr4:56593845..56596121-chr4:56598605..56600878,2	K562	blood:
46	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:
47	chr4:56479641..56481239-chr4:56491828..56493480,2	K562	blood:
48	chr4:56531998..56534382-chr4:56600029..56601817,2	K562	blood:
49	chr4:56492997..56495090-chr4:56501850..56503549,2	K562	blood:
50	chr4:56492253..56496567-chr4:56500430..56503372,5	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-1	chr4:56496569-56496627	NONHSAT096475
2	lnc-NMU-1	chr4:56496569-56496629	NONHSAT096476
3	lnc-NMU-2	chr4:56508763-56508927	l_2648_chr4:56499345-56508927_adipose
4	lnc-NMU-2	chr4:56501440-56501555	l_2648_chr4:56499345-56508927_adipose
5	lnc-NMU-2	chr4:56499346-56499878	l_2648_chr4:56499345-56508927_adipose
6	lnc-NMU-1	chr4:56502711-56502865	NONHSAT096475

No data

Variant related genes	Relation type
NMU	TF binding region
NMU	CpG island
ENSG00000090989	chromatin interactions
ENSG00000134851	chromatin interactions
ENSG00000128039	chromatin interactions
ENSG00000134852	chromatin interactions
ENSG00000109255	chromatin interactions
ENSG00000272969	chromatin interactions

Extended variants
information (count: 4548 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4548 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3805389	chr4:56482750-56482751	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563830367	chr4:56482765-56482766	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113930677	chr4:56482821-56482822	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138300823	chr4:56482844-56482845	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533704954	chr4:56482884-56482885	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559274661	chr4:56483052-56483053	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149520148	chr4:56483072-56483073	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185624803	chr4:56483077-56483078	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146977150	chr4:56483098-56483099	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534684459	chr4:56483139-56483140	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569599305	chr4:56483167-56483168	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571508340	chr4:56483182-56483183	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28434262	chr4:56483222-56483223	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs373598709	chr4:56483259-56483260	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143709155	chr4:56483270-56483271	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61072181	chr4:56483377-56483378	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs563808084	chr4:56483386-56483387	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548658350	chr4:56483387-56483388	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555496974	chr4:56483444-56483445	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs3811826	chr4:56483538-56483539	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs536548102	chr4:56483544-56483545	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534833001	chr4:56483570-56483571	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187818458	chr4:56483590-56483591	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375954015	chr4:56483608-56483609	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557830843	chr4:56483609-56483610	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147079985	chr4:56483674-56483675	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201759371	chr4:56483693-56483694	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191972677	chr4:56483727-56483728	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543619419	chr4:56483728-56483729	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141367148	chr4:56483761-56483762	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73236165	chr4:56483784-56483785	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs561849736	chr4:56483789-56483790	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562756950	chr4:56483796-56483797	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144383831	chr4:56483801-56483802	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150791222	chr4:56483802-56483803	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371959000	chr4:56483876-56483877	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184349294	chr4:56483884-56483885	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188391521	chr4:56483890-56483891	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112867528	chr4:56483907-56483908	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139485931	chr4:56483922-56483923	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530576934	chr4:56483977-56483978	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550516362	chr4:56484062-56484063	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35233725	chr4:56484183-56484184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571094873	chr4:56484205-56484206	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567424193	chr4:56484237-56484238	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529980925	chr4:56484238-56484239	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546865137	chr4:56484293-56484294	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565989402	chr4:56484297-56484298	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534703074	chr4:56484311-56484312	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538587236	chr4:56484332-56484333	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56473600-56491600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:56476200-56485000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:56478200-56491600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:56478600-56485000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:56481000-56483400	Genic enhancers	K562	blood
6	chr4:56481600-56485200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:56483400-56484200	Enhancers	K562	blood
8	chr4:56483600-56484200	Enhancers	GM12878-XiMat	blood
9	chr4:56484200-56491600	Weak transcription	K562	blood
10	chr4:56484400-56484800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:56484800-56485000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:56485000-56485200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:56485000-56485400	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr4:56485000-56485400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr4:56485000-56485400	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr4:56485000-56485400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr4:56485000-56485400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:56485200-56485400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:56485200-56487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:56485200-56491400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:56485400-56491800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:56485400-56491800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr4:56485400-56498000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:56485400-56498400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr4:56489400-56493800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:56489400-56498000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:56489800-56498200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:56491400-56492200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:56491600-56492400	ZNF genes & repeats	K562	blood
30	chr4:56491600-56492600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:56491600-56496200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:56491800-56492200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
33	chr4:56491800-56493400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr4:56492000-56492200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:56492000-56492200	Enhancers	Esophagus	oesophagus
36	chr4:56492000-56496400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:56492200-56495800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:56492200-56498200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr4:56492200-56498200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:56492400-56496600	Strong transcription	K562	blood
41	chr4:56492600-56498400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr4:56493400-56500200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr4:56493800-56494600	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:56494000-56500600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr4:56494600-56495200	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:56495200-56496200	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr4:56495800-56499000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:56496200-56498200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr4:56496200-56498800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:56496600-56497000	Transcr. at gene 5' and 3'	K562	blood

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