Variant report

Variant	nsv932636
Chromosome Location	chr4:56438618-56667329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1656)
CpG islands
(count:2691)
Chromatin interactive
region (count:154)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56602401-56602562	K562	blood:	n/a	n/a
2	ARID3A	chr4:56599903-56600328	K562	blood:	n/a	n/a
3	ARID3A	chr4:56474539-56474545	K562	blood:	n/a	n/a
4	ARID3A	chr4:56535243-56535280	K562	blood:	n/a	n/a
5	ARID3A	chr4:56519920-56520587	K562	blood:	n/a	n/a
6	ARID3A	chr4:56602788-56603227	K562	blood:	n/a	n/a
7	ARID3A	chr4:56501495-56501827	K562	blood:	n/a	n/a
8	ARID3A	chr4:56595714-56597053	K562	blood:	n/a	n/a
9	ARID3A	chr4:56602821-56603153	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:56503388-56504015	K562	blood:	n/a	n/a
11	ARID3A	chr4:56589584-56589800	K562	blood:	n/a	n/a
12	ARID3A	chr4:56493426-56493494	K562	blood:	n/a	n/a
13	ARID3A	chr4:56608965-56609070	K562	blood:	n/a	n/a
14	ARID3A	chr4:56515038-56515098	K562	blood:	n/a	n/a
15	ARID3A	chr4:56536930-56537271	K562	blood:	n/a	n/a
16	ARID3A	chr4:56597276-56597725	K562	blood:	n/a	n/a
17	ARID3A	chr4:56518503-56518691	K562	blood:	n/a	n/a
18	ATF1	chr4:56595957-56597096	K562	blood:	n/a	n/a
19	ATF1	chr4:56498147-56498454	K562	blood:	n/a	n/a
20	ATF1	chr4:56501416-56501837	K562	blood:	n/a	n/a
21	ATF1	chr4:56536954-56537234	K562	blood:	n/a	n/a
22	ATF3	chr4:56600082-56600281	K562	blood:	n/a	n/a
23	ATF3	chr4:56599950-56600410	K562	blood:	n/a	n/a
24	ATF3	chr4:56634460-56634806	K562	blood:	n/a	n/a
25	BACH1	chr4:56479913-56479931	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:56503593-56503801	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:56539608-56539938	K562	blood:	n/a	n/a
28	BACH1	chr4:56502324-56502563	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:56502806-56503160	H1-hESC	embryonic stem cell:	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	BACH1	chr4:56503675-56503978	K562	blood:	n/a	n/a
33	BACH1	chr4:56483945-56484132	K562	blood:	n/a	n/a
34	BATF	chr4:56483976-56484328	GM12878	blood:	n/a	n/a
35	BATF	chr4:56483933-56484337	GM12878	blood:	n/a	n/a
36	BCL3	chr4:56458572-56459349	K562	blood:	n/a	n/a
37	BCL3	chr4:56459850-56460592	K562	blood:	n/a	chr4:56460261-56460270
38	BHLHE40	chr4:56504145-56504547	K562	blood:	n/a	n/a
39	BHLHE40	chr4:56595973-56597056	K562	blood:	n/a	n/a
40	BHLHE40	chr4:56589634-56589918	K562	blood:	n/a	n/a
41	BHLHE40	chr4:56502266-56502629	K562	blood:	n/a	n/a
42	BHLHE40	chr4:56501226-56501818	K562	blood:	n/a	n/a
43	BHLHE40	chr4:56602362-56602445	K562	blood:	n/a	n/a
44	BHLHE40	chr4:56600069-56600344	K562	blood:	n/a	n/a
45	BHLHE40	chr4:56520557-56520573	K562	blood:	n/a	n/a
46	BHLHE40	chr4:56608920-56609395	K562	blood:	n/a	n/a
47	BRCA1	chr4:56620954-56621308	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr4:56441586-56442153	HCT-116	colon:	n/a	n/a
49	CBX3	chr4:56441655-56442059	K562	blood:	n/a	n/a
50	CBX3	chr4:56475764-56476183	HCT-116	colon:	n/a	n/a

(count:2691 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56534223-56534273	U87	brain:	n/a
2	chr4:56504657-56504707	MCF10A-Er-Src	breast:	n/a
3	chr4:56663994-56664044	PFSK-1	brain:	n/a
4	chr4:56659922-56659972	NH-A	brain:	n/a
5	chr4:56458622-56458672	HAEpiC	amniotic membrane:	n/a
6	chr4:56502849-56502899	SK-N-SH	brain:	n/a
7	chr4:56660328-56660378	Jurkat	blood:	n/a
8	chr4:56534223-56534273	U87	brain:	n/a
9	chr4:56504657-56504707	MCF10A-Er-Src	breast:	n/a
10	chr4:56663994-56664044	PFSK-1	brain:	n/a
11	chr4:56659922-56659972	NH-A	brain:	n/a
12	chr4:56458622-56458672	HAEpiC	amniotic membrane:	n/a
13	chr4:56502849-56502899	SK-N-SH	brain:	n/a
14	chr4:56660328-56660378	Jurkat	blood:	n/a
15	chr4:56658357-56658407	NHBE	bronchial:	n/a
16	chr4:56504657-56504707	RPTEC	kidney:	n/a
17	chr4:56502392-56502442	HCT-116	colon:	n/a
18	chr4:56501727-56501777	HCT-116	colon:	n/a
19	chr4:56502534-56502584	HRE	kidney:	n/a
20	chr4:56458183-56458233	MCF10A-Er-Src	breast:	n/a
21	chr4:56501441-56501491	HCM	heart:	n/a
22	chr4:56458333-56458383	Hepatocyte	liver:	n/a
23	chr4:56660328-56660378	SKMC	muscle:	n/a
24	chr4:56659985-56660035	HMEC	breast:	n/a
25	chr4:56659924-56659974	MCF-7	breast:	n/a
26	chr4:56500362-56500412	BJ	skin:	n/a
27	chr4:56458449-56458499	H1-hESC	embryonic stem cell:	embryo
28	chr4:56534223-56534273	HMEC	breast:	n/a
29	chr4:56502898-56502948	HNPCEpiC	eye:	n/a
30	chr4:56458513-56458563	NH-A	brain:	n/a
31	chr4:56502664-56502714	NT2-D1	testis:	n/a
32	chr4:56464927-56464977	SK-N-SH	brain:	n/a
33	chr4:56502864-56502914	HCM	heart:	n/a
34	chr4:56439270-56439320	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:56660143-56660193	HNPCEpiC	eye:	n/a
36	chr4:56502788-56502838	K562	blood:	n/a
37	chr4:56475905-56475955	MCF-7	breast:	n/a
38	chr4:56458333-56458383	K562	blood:	n/a
39	chr4:56656788-56656838	HepG2	liver:	n/a
40	chr4:56660143-56660193	AG10803	skin:	n/a
41	chr4:56458183-56458233	ovcar-3	ovarian:	n/a
42	chr4:56659770-56659820	SK-N-SH	brain:	n/a
43	chr4:56660328-56660378	NH-A	brain:	n/a
44	chr4:56660398-56660448	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:56502664-56502714	BE2_C	brain:	n/a
46	chr4:56504657-56504707	A549	lung:	n/a
47	chr4:56659770-56659820	NH-A	brain:	n/a
48	chr4:56496836-56496886	SKMC	muscle:	n/a
49	chr4:56502664-56502714	SK-N-SH	brain:	n/a
50	chr4:56458511-56458561	NH-A	brain:	n/a

(count:154 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:
2	chr4:56522244..56525288-chr4:56525318..56527795,3	K562	blood:
3	chr4:56504870..56506522-chr4:56515627..56517625,2	K562	blood:
4	chr4:56613502..56615482-chr4:56616796..56619425,2	K562	blood:
5	chr4:56523921..56526378-chr4:56528208..56530318,2	K562	blood:
6	chr4:56474369..56476951-chr4:56481028..56484786,4	K562	blood:
7	chr4:56462852..56464632-chr4:56730445..56733358,2	K562	blood:
8	chr4:56532999..56536054-chr4:56538312..56541698,3	K562	blood:
9	chr4:56520187..56522696-chr4:56535355..56536879,2	K562	blood:
10	chr4:56531998..56534382-chr4:56600029..56601817,2	K562	blood:
11	chr4:56587276..56591232-chr4:56591490..56593918,4	K562	blood:
12	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
13	chr4:56631564..56634040-chr4:56635751..56638538,2	K562	blood:
14	chr4:56460832..56462856-chr4:56478236..56479860,2	MCF-7	breast:
15	chr4:56520164..56522203-chr4:56529132..56532078,2	K562	blood:
16	chr4:56550080..56552632-chr4:56586091..56588809,2	K562	blood:
17	chr4:56637542..56640482-chr4:56658130..56659977,2	K562	blood:
18	chr4:56480747..56484464-chr4:56594012..56597947,4	K562	blood:
19	chr4:56272858..56275843-chr4:56602241..56604494,2	K562	blood:
20	chr4:56412086..56414460-chr4:56599995..56602256,4	MCF-7	breast:
21	chr4:56512381..56514282-chr4:56518613..56520259,2	K562	blood:
22	chr4:56517756..56519698-chr4:56525326..56526892,2	K562	blood:
23	chr4:56512523..56514282-chr4:56518613..56521303,2	K562	blood:
24	chr4:56411908..56414251-chr4:56442457..56445363,2	K562	blood:
25	chr4:56481534..56484408-chr4:56607415..56610057,2	K562	blood:
26	chr4:56466882..56469712-chr4:56475375..56477433,2	K562	blood:
27	chr4:56587276..56591232-chr4:56591490..56593918,4	K562	blood:
28	chr4:56649556..56651202-chr4:56652557..56654365,2	K562	blood:
29	chr4:56479641..56482011-chr4:56491746..56493328,2	K562	blood:
30	chr4:56434047..56435650-chr4:56438731..56441489,2	K562	blood:
31	chr4:56459983..56461740-chr4:56464229..56467052,3	K562	blood:
32	chr4:56507649..56509909-chr4:56526051..56528840,3	K562	blood:
33	chr4:56212321..56212921-chr4:56602569..56603071,2	K562	blood:
34	chr4:56512523..56514282-chr4:56518613..56521303,2	K562	blood:
35	chr4:56637771..56639865-chr4:56697633..56699417,2	MCF-7	breast:
36	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:
37	chr4:56596053..56598450-chr4:56609132..56610849,2	K562	blood:
38	chr4:56474369..56476951-chr4:56481028..56484786,4	K562	blood:
39	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
40	chr4:56520164..56522203-chr4:56529132..56532078,2	K562	blood:
41	chr4:56501844..56503895-chr4:56534983..56537847,2	K562	blood:
42	chr4:56466882..56469712-chr4:56475375..56477433,2	K562	blood:
43	chr4:56597356..56599483-chr4:56719674..56722401,2	K562	blood:
44	chr4:56472523..56475869-chr4:56480434..56484043,4	K562	blood:
45	chr4:56567077..56569612-chr4:56570589..56573149,3	K562	blood:
46	chr4:56609301..56611255-chr4:56614835..56616393,2	MCF-7	breast:
47	chr4:56498450..56502811-chr4:56593362..56599516,6	K562	blood:
48	chr4:56303798..56306133-chr4:56600360..56603061,2	K562	blood:
49	chr4:56527671..56530669-chr4:56531905..56533687,2	K562	blood:
50	chr4:56593845..56596121-chr4:56598605..56600878,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-1	chr4:56473604-56473633	NONHSAT096475
2	lnc-NMU-1	chr4:56502711-56502865	NONHSAT096475
3	lnc-NMU-1	chr4:56466689-56466742	NONHSAT096476
4	lnc-NMU-1	chr4:56465309-56465348	NONHSAT096475
5	lnc-NMU-1	chr4:56496569-56496629	NONHSAT096476
6	lnc-NMU-1	chr4:56482505-56482552	NONHSAT096475
7	lnc-NMU-1	chr4:56465319-56465348	NONHSAT096476
8	lnc-NMU-1	chr4:56461484-56461578	NONHSAT096475
9	lnc-NMU-1	chr4:56496569-56496627	NONHSAT096475
10	lnc-NMU-1	chr4:56473604-56473633	NONHSAT096476
11	lnc-NMU-1	chr4:56482505-56482552	NONHSAT096476
12	lnc-NMU-1	chr4:56475287-56475346	NONHSAT096476
13	lnc-NMU-2	chr4:56499346-56499878	l_2648_chr4:56499345-56508927_adipose
14	lnc-NMU-1	chr4:56466689-56466742	NONHSAT096475
15	lnc-NMU-2	chr4:56501440-56501555	l_2648_chr4:56499345-56508927_adipose
16	lnc-NMU-1	chr4:56471442-56471516	NONHSAT096475
17	lnc-NMU-2	chr4:56508763-56508927	l_2648_chr4:56499345-56508927_adipose
18	lnc-NMU-1	chr4:56475287-56475346	NONHSAT096475

No data

Variant related genes	Relation type
NMU	TF binding region
RNU6-276P	TF binding region
PDCL2	TF binding region
NMU	CpG island
RNU6-276P	CpG island
PDCL2	CpG island
ENSG00000128039	chromatin interactions
ENSG00000272969	chromatin interactions
ENSG00000090989	chromatin interactions
ENSG00000134852	chromatin interactions
ENSG00000134851	chromatin interactions
ENSG00000109255	chromatin interactions

Extended variants
information (count: 6500 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:6500 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368773016	chr4:56438627-56438628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76786566	chr4:56438651-56438652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564736426	chr4:56438700-56438701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192510485	chr4:56438735-56438736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62310862	chr4:56438761-56438762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569695885	chr4:56438801-56438802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535522256	chr4:56438809-56438810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577954565	chr4:56438835-56438836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377067102	chr4:56438847-56438848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565541434	chr4:56438848-56438849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545558586	chr4:56438929-56438930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201401278	chr4:56438933-56438934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149571227	chr4:56438941-56438942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534482304	chr4:56438996-56438997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368401016	chr4:56439019-56439020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557644954	chr4:56439028-56439029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577852898	chr4:56439064-56439065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372195451	chr4:56439071-56439072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533599977	chr4:56439080-56439081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546855356	chr4:56439095-56439096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530978955	chr4:56439135-56439136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12171430	chr4:56439166-56439167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7665678	chr4:56439216-56439217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576318078	chr4:56439220-56439221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542346410	chr4:56439221-56439222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7665846	chr4:56439245-56439246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184624933	chr4:56439253-56439254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541624911	chr4:56439256-56439257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147720194	chr4:56439291-56439292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561496893	chr4:56439293-56439294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533671946	chr4:56439362-56439363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543088254	chr4:56439429-56439430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117841700	chr4:56439465-56439466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528835146	chr4:56439527-56439528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548689742	chr4:56439560-56439561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565401521	chr4:56439565-56439566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528304052	chr4:56439586-56439587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34534635	chr4:56439591-56439592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs571492912	chr4:56439627-56439628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141028985	chr4:56439673-56439674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555785793	chr4:56439715-56439716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570056290	chr4:56439760-56439761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528800765	chr4:56439763-56439764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535817002	chr4:56439774-56439775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547247775	chr4:56439798-56439799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6848755	chr4:56439812-56439813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572552366	chr4:56439831-56439832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541690493	chr4:56439899-56439900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538246787	chr4:56439958-56439959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201924394	chr4:56440013-56440014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56432000-56442000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:56435200-56440600	Weak transcription	K562	blood
3	chr4:56435600-56441400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:56439000-56440800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:56440600-56441200	Strong transcription	K562	blood
6	chr4:56440800-56441600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:56441200-56464400	Weak transcription	K562	blood
8	chr4:56441600-56443400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:56444000-56444200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr4:56444200-56444800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr4:56444200-56445600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr4:56444800-56445200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:56445200-56445400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr4:56445400-56445600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr4:56449800-56450000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:56450000-56450800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:56454200-56454600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr4:56454400-56454800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:56454400-56454800	Enhancers	Fetal Lung	lung
20	chr4:56455800-56456200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:56456200-56458400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:56458000-56458400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:56458200-56458600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:56458200-56458600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:56458400-56458600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:56458400-56458600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:56458600-56458800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:56458600-56460000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:56458600-56463800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:56460000-56464800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:56461200-56464600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:56463800-56467000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:56464200-56475800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:56464400-56468800	Strong transcription	K562	blood
35	chr4:56464600-56465600	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:56464800-56465400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:56465400-56479400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:56465600-56476000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr4:56467000-56468400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:56468400-56469400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:56468800-56470400	Weak transcription	K562	blood
42	chr4:56469400-56470200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:56469800-56481200	Weak transcription	Esophagus	oesophagus
44	chr4:56470200-56472400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:56470400-56478800	Strong transcription	K562	blood
46	chr4:56471400-56471800	Enhancers	Fetal Muscle Leg	muscle
47	chr4:56472400-56476600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr4:56473600-56491600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr4:56474000-56475800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:56474400-56475200	Enhancers	HMEC	breast

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