Variant report

Variant	nsv1007114
Chromosome Location	chr4:56942917-57055381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:912)
CpG islands
(count:306)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56952324-56952670	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:57000348-57000651	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:56999175-56999293	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:56970225-56970838	HepG2	liver:	n/a	n/a
5	ATF1	chr4:57047391-57048010	K562	blood:	n/a	n/a
6	ATF1	chr4:57024759-57024993	K562	blood:	n/a	n/a
7	ATF3	chr4:57024757-57024966	K562	blood:	n/a	chr4:57024888-57024901 chr4:57024887-57024902
8	ATF3	chr4:56995656-56995891	K562	blood:	n/a	n/a
9	ATF3	chr4:57049527-57049775	K562	blood:	n/a	n/a
10	BACH1	chr4:56995571-56995985	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:57013668-57013991	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:57019003-57019017	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:56973718-56973985	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:57013663-57013995	K562	blood:	n/a	n/a
15	BATF	chr4:56996934-56997217	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:57049712-57050079	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:56995704-56995850	K562	blood:	n/a	n/a
18	BHLHE40	chr4:56952512-56952612	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:57049526-57049852	K562	blood:	n/a	n/a
20	BRCA1	chr4:56978643-56978678	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:56946625-56946824	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr4:56952716-56952963	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr4:57049530-57049892	K562	blood:	n/a	n/a
24	CBX3	chr4:57049542-57049915	K562	blood:	n/a	n/a
25	CCNT2	chr4:56976554-56976654	K562	blood:	n/a	n/a
26	CEBPB	chr4:56952302-56952686	HepG2	liver:	n/a	chr4:56952499-56952510
27	CEBPB	chr4:56952316-56952700	H1-hESC	embryonic stem cell:	n/a	chr4:56952499-56952510
28	CEBPB	chr4:56970276-56970637	HepG2	liver:	n/a	chr4:56970510-56970521
29	CEBPB	chr4:56946466-56946832	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:56953393-56953656	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:56988264-56988535	K562	blood:	n/a	chr4:56988369-56988382 chr4:56988370-56988381 chr4:56988369-56988380
32	CEBPB	chr4:56952439-56952533	IMR90	lung:	n/a	chr4:56952499-56952510
33	CEBPB	chr4:57015861-57016083	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:57001102-57001512	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:56970322-56970651	HepG2	liver:	n/a	chr4:56970510-56970521
36	CEBPB	chr4:57014675-57014942	Hela-S3	cervix:	n/a	chr4:57014827-57014844
37	CEBPB	chr4:56952380-56952599	K562	blood:	n/a	chr4:56952499-56952510
38	CEBPB	chr4:56993785-56994037	HepG2	liver:	n/a	chr4:56993883-56993894 chr4:56993882-56993895
39	CEBPB	chr4:56952168-56953080	Hela-S3	cervix:	n/a	chr4:56952499-56952510
40	CEBPB	chr4:56958520-56958744	HepG2	liver:	n/a	chr4:56958670-56958681
41	CEBPB	chr4:57047438-57047638	K562	blood:	n/a	n/a
42	CEBPB	chr4:56946018-56946206	A549	lung:	n/a	chr4:56946119-56946130
43	CEBPB	chr4:56961738-56961878	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:56999163-56999259	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:56970397-56970620	HepG2	liver:	n/a	chr4:56970510-56970521
46	CEBPB	chr4:57000044-57000083	HepG2	liver:	n/a	chr4:57000051-57000062
47	CEBPB	chr4:56970352-56970690	HepG2	liver:	n/a	chr4:56970510-56970521
48	CEBPB	chr4:56988231-56988504	HepG2	liver:	n/a	chr4:56988369-56988382 chr4:56988370-56988381 chr4:56988369-56988380
49	CEBPB	chr4:56945968-56946254	HepG2	liver:	n/a	chr4:56946119-56946130
50	CEBPB	chr4:57047457-57047670	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56978667-56978717	Hepatocyte	liver:	n/a
2	chr4:56978667-56978717	Hepatocyte	liver:	n/a
3	chr4:57035957-57036007	HepG2	liver:	n/a
4	chr4:57035957-57036007	HCM	heart:	n/a
5	chr4:57036403-57036453	SAEC	small airway:	n/a
6	chr4:56978667-56978717	HIPEpiC	eye:	n/a
7	chr4:57035957-57036007	ProgFib	skin:	n/a
8	chr4:56978667-56978717	GM12892	blood:	n/a
9	chr4:57036298-57036348	A549	lung:	n/a
10	chr4:57036403-57036453	NH-A	brain:	n/a
11	chr4:57035957-57036007	Hela-S3	cervix:	n/a
12	chr4:57036403-57036453	AoSMC	blood vessel:	n/a
13	chr4:56978667-56978717	Hela-S3	cervix:	n/a
14	chr4:57036403-57036453	CMK	blood:	n/a
15	chr4:57036298-57036348	AoSMC	blood vessel:	n/a
16	chr4:57036298-57036348	NH-A	brain:	n/a
17	chr4:57035948-57035998	SK-N-SH_RA	brain:	n/a
18	chr4:57036403-57036453	AG04449	skin:	fetal
19	chr4:57036298-57036348	SAEC	small airway:	n/a
20	chr4:57036403-57036453	HEK293	kidney:	embryo
21	chr4:57035957-57036007	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:57035957-57036007	HRE	kidney:	n/a
23	chr4:57035948-57035998	NT2-D1	testis:	n/a
24	chr4:57036298-57036348	HUVEC	blood vessel:	n/a
25	chr4:57035957-57036007	NH-A	brain:	n/a
26	chr4:57036403-57036453	PANC-1	pancreas:	n/a
27	chr4:57035948-57035998	AG09309	skin:	n/a
28	chr4:57035957-57036007	GM06990	blood:	n/a
29	chr4:57035948-57035998	H1-hESC	embryonic stem cell:	embryo
30	chr4:57035957-57036007	GM12878	blood:	n/a
31	chr4:57035948-57035998	HUVEC	blood vessel:	n/a
32	chr4:57035948-57035998	AG04449	skin:	fetal
33	chr4:56978667-56978717	PrEC	prostate:	n/a
34	chr4:57036298-57036348	PrEC	prostate:	n/a
35	chr4:57035948-57035998	BJ	skin:	n/a
36	chr4:57036298-57036348	HIPEpiC	eye:	n/a
37	chr4:57036298-57036348	GM12891	blood:	n/a
38	chr4:57035957-57036007	HEK293	kidney:	embryo
39	chr4:57036403-57036453	K562	blood:	n/a
40	chr4:57036403-57036453	AG09309	skin:	n/a
41	chr4:57036403-57036453	HAEpiC	amniotic membrane:	n/a
42	chr4:56978667-56978717	PFSK-1	brain:	n/a
43	chr4:57035948-57035998	BE2_C	brain:	n/a
44	chr4:57035957-57036007	T-47D	breast:	n/a
45	chr4:57035948-57035998	LNCaP	prostate:	n/a
46	chr4:57036403-57036453	HCF	heart:	n/a
47	chr4:57035948-57035998	SK-N-SH	brain:	n/a
48	chr4:56978667-56978717	HMEC	breast:	n/a
49	chr4:56978667-56978717	SK-N-SH_RA	brain:	n/a
50	chr4:57035957-57036007	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:56995263..56996196-chr4:57049303..57050160,2	K562	blood:
2	chr4:57009940..57012315-chr4:57015568..57017810,2	K562	blood:
3	chr4:57009940..57012315-chr4:57015568..57017810,2	K562	blood:
4	chr4:56995303..56996217-chr4:57702535..57703041,2	MCF-7	breast:
5	chr4:56986755..56988749-chr4:56988899..56991340,2	MCF-7	breast:
6	chr4:56996872..56999249-chr4:57000156..57002361,2	K562	blood:
7	chr4:56914423..56917343-chr4:56954991..56956586,2	MCF-7	breast:
8	chr4:56994960..56996210-chr4:57167032..57168215,14	MCF-7	breast:
9	chr4:57024723..57027325-chr4:57027371..57029147,2	MCF-7	breast:
10	chr4:57021309..57023973-chr4:57025557..57028531,2	K562	blood:
11	chr4:56791515..56793046-chr4:56992694..56994388,2	K562	blood:
12	chr4:56990498..56992393-chr4:56995607..56997336,2	K562	blood:
13	chr4:56996872..56999249-chr4:57000156..57002361,2	K562	blood:
14	chr4:57046901..57049380-chr4:57055137..57059248,3	K562	blood:
15	chr4:57046901..57049380-chr4:57055137..57059248,3	K562	blood:
16	chr4:56915544..56917169-chr4:56971414..56974217,2	K562	blood:
17	chr4:57020491..57022913-chr4:57025333..57027120,2	K562	blood:
18	chr4:57054944..57056829-chr4:57061059..57063842,2	MCF-7	breast:
19	chr4:57024723..57027325-chr4:57027371..57029147,2	MCF-7	breast:
20	chr4:56986755..56988749-chr4:56988899..56991340,2	MCF-7	breast:
21	chr4:56944085..56946867-chr4:56949220..56951165,2	K562	blood:
22	chr4:56947441..56950435-chr4:56956145..56959443,3	K562	blood:
23	chr4:56960470..56963101-chr4:56964832..56967339,3	MCF-7	breast:
24	chr4:57026944..57028463-chr4:57029397..57031028,2	K562	blood:
25	chr4:57026944..57028463-chr4:57029397..57031028,2	K562	blood:
26	chr4:57020491..57022913-chr4:57025333..57027120,2	K562	blood:
27	chr4:56960470..56963101-chr4:56964832..56967339,3	MCF-7	breast:
28	chr4:56947441..56950435-chr4:56956145..56959443,3	K562	blood:
29	chr4:56990498..56992393-chr4:56995607..56997336,2	K562	blood:
30	chr4:57007519..57009026-chr4:57014142..57015746,2	K562	blood:
31	chr4:57007519..57009026-chr4:57014142..57015746,2	K562	blood:
32	chr4:56944085..56946867-chr4:56949220..56951165,2	K562	blood:
33	chr4:56995235..56996245-chr4:57167093..57168027,4	MCF-7	breast:
34	chr4:57021309..57023973-chr4:57025557..57028531,2	K562	blood:
35	chr4:56995263..56996196-chr4:57049303..57050160,2	K562	blood:

No data

Variant related genes	Relation type
KIAA1211	TF binding region
RNA5SP161	TF binding region
KIAA1211	CpG island
RNA5SP161	CpG island

Extended variants
information (count: 4113 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4113 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80299972	chr4:56942943-56942944	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567867264	chr4:56943011-56943012	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs565386805	chr4:56943017-56943018	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs372507908	chr4:56943047-56943048	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs534426241	chr4:56943065-56943066	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs368656603	chr4:56943093-56943094	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs574938724	chr4:56943159-56943160	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs534366881	chr4:56943264-56943265	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs144807702	chr4:56943276-56943277	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs139960110	chr4:56943334-56943335	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs571048150	chr4:56943335-56943336	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs573869931	chr4:56943337-56943338	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs372017094	chr4:56943339-56943340	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs145477593	chr4:56943384-56943385	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs553214009	chr4:56943393-56943394	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs77142826	chr4:56943402-56943403	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs372139154	chr4:56943409-56943410	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs572469582	chr4:56943417-56943418	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs114379752	chr4:56943431-56943432	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs564485778	chr4:56943434-56943435	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs35786306	chr4:56943442-56943443	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs58927874	chr4:56943449-56943450	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs75408956	chr4:56943483-56943484	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529548832	chr4:56943486-56943487	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs369912572	chr4:56943489-56943490	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs192975877	chr4:56943531-56943532	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs566155698	chr4:56943547-56943548	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs528158529	chr4:56943555-56943556	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs372946613	chr4:56943584-56943585	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs571205486	chr4:56943604-56943605	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs536687104	chr4:56943606-56943607	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs78855266	chr4:56943674-56943675	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs567520953	chr4:56943727-56943728	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs373956608	chr4:56943728-56943729	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs182631309	chr4:56943762-56943763	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs538539936	chr4:56943874-56943875	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572983559	chr4:56943885-56943886	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541501052	chr4:56943892-56943893	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558011932	chr4:56943908-56943909	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113693406	chr4:56943911-56943912	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187329356	chr4:56943946-56943947	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75898201	chr4:56943983-56943984	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563348368	chr4:56944007-56944008	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17742722	chr4:56944016-56944017	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542933797	chr4:56944041-56944042	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6554328	chr4:56944109-56944110	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528712598	chr4:56944154-56944155	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150346539	chr4:56944197-56944198	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559877295	chr4:56944292-56944293	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146494985	chr4:56944303-56944304	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56931200-56943600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:56935400-56945000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:56936000-56943800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:56941800-56943200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:56941800-56943800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:56941800-56945400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr4:56941800-56945600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:56942400-56944200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:56942400-56947000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:56942800-56943000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:56942800-56945200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:56943200-56946200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
13	chr4:56943600-56944000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:56943600-56945000	Enhancers	Hela-S3	cervix
15	chr4:56943800-56944000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
16	chr4:56943800-56944000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:56944000-56944600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:56944000-56945000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr4:56944200-56951000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:56944600-56945600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:56944800-56945200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr4:56944800-56945200	Weak transcription	Right Atrium	heart
23	chr4:56945000-56945200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:56945000-56945400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:56945000-56945400	Flanking Active TSS	Hela-S3	cervix
26	chr4:56945200-56945400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:56945200-56945400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:56945200-56945400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:56945200-56945400	Enhancers	Right Atrium	heart
30	chr4:56945200-56945800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:56945200-56946000	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:56945200-56948400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr4:56945200-56951800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:56945400-56945600	Weak transcription	Fetal Brain Female	brain
35	chr4:56945400-56946600	Enhancers	Hela-S3	cervix
36	chr4:56945400-56948600	Weak transcription	Brain Germinal Matrix	brain
37	chr4:56945400-56949000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:56945400-56950800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:56945400-56951000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:56945400-56952200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:56945600-56948200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:56945600-56965200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:56945800-56950200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:56946000-56946800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr4:56946200-56947000	Strong transcription	Primary hematopoietic stem cells	blood
46	chr4:56946600-56950800	Weak transcription	Hela-S3	cervix
47	chr4:56946800-56947000	Enhancers	Fetal Intestine Small	intestine
48	chr4:56946800-56947200	Enhancers	Duodenum Mucosa	Duodenum
49	chr4:56946800-56947600	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:56947000-56947400	Weak transcription	Primary hematopoietic stem cells	blood

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