Variant report

Variant	esv2763801
Chromosome Location	chr4:99094892-99413853
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2472)
CpG islands
(count:1588)
Chromatin interactive
region (count:143)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2472 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99174738-99175080	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:99392142-99392351	K562	blood:	n/a	n/a
3	ARID3A	chr4:99239639-99239936	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:99153553-99153558	K562	blood:	n/a	n/a
5	ARID3A	chr4:99308616-99309381	K562	blood:	n/a	n/a
6	ARID3A	chr4:99183740-99183927	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:99388747-99389025	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:99182631-99182760	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:99388619-99388998	K562	blood:	n/a	n/a
10	ARID3A	chr4:99182185-99182418	HepG2	liver:	n/a	n/a
11	ATF1	chr4:99153376-99153775	K562	blood:	n/a	n/a
12	ATF1	chr4:99383753-99383806	K562	blood:	n/a	n/a
13	ATF2	chr4:99400713-99401148	GM12878	blood:	n/a	n/a
14	ATF2	chr4:99403935-99404529	GM12878	blood:	n/a	n/a
15	ATF2	chr4:99400704-99401157	GM12878	blood:	n/a	n/a
16	ATF2	chr4:99367698-99368543	GM12878	blood:	n/a	n/a
17	ATF2	chr4:99403734-99404509	GM12878	blood:	n/a	n/a
18	ATF2	chr4:99367519-99368646	GM12878	blood:	n/a	n/a
19	ATF2	chr4:99181655-99182496	GM12878	blood:	n/a	n/a
20	ATF3	chr4:99153321-99153783	K562	blood:	n/a	n/a
21	ATF3	chr4:99153348-99153854	HCT-116	colon:	n/a	n/a
22	BACH1	chr4:99181738-99183321	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr4:99320220-99320335	K562	blood:	n/a	n/a
24	BACH1	chr4:99388764-99389070	K562	blood:	n/a	n/a
25	BACH1	chr4:99388711-99389161	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:99208547-99208551	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr4:99403975-99404403	GM12878	blood:	n/a	n/a
28	BATF	chr4:99125451-99125672	GM12878	blood:	n/a	n/a
29	BATF	chr4:99184897-99185129	GM12878	blood:	n/a	chr4:99185019-99185030
30	BATF	chr4:99124532-99124841	GM12878	blood:	n/a	n/a
31	BATF	chr4:99367606-99368035	GM12878	blood:	n/a	chr4:99367801-99367812
32	BATF	chr4:99400666-99401089	GM12878	blood:	n/a	chr4:99400913-99400924
33	BATF	chr4:99388800-99389008	GM12878	blood:	n/a	n/a
34	BATF	chr4:99351956-99352132	GM12878	blood:	n/a	chr4:99352058-99352069 chr4:99352031-99352042
35	BATF	chr4:99400722-99401006	GM12878	blood:	n/a	chr4:99400913-99400924
36	BATF	chr4:99403859-99404731	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:99403973-99404414	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:99124533-99125120	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:99400753-99401097	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:99404041-99404324	GM12878	blood:	n/a	n/a
41	BCL11A	chr4:99125383-99125694	GM12878	blood:	n/a	chr4:99125514-99125523
42	BCL11A	chr4:99368312-99368517	GM12878	blood:	n/a	n/a
43	BCL3	chr4:99404300-99405170	A549	lung:	n/a	n/a
44	BCL3	chr4:99403961-99404763	GM12878	blood:	n/a	n/a
45	BCLAF1	chr4:99388655-99389080	GM12878	blood:	n/a	n/a
46	BCLAF1	chr4:99367527-99368477	GM12878	blood:	n/a	chr4:99367804-99367813
47	BHLHE40	chr4:99183157-99183490	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:99367501-99368551	GM12878	blood:	n/a	n/a
49	BHLHE40	chr4:99182731-99182932	GM12878	blood:	n/a	n/a
50	BHLHE40	chr4:99404008-99404297	GM12878	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99235909-99235959	MCF-7	breast:	n/a
2	chr4:99182798-99182848	GM12891	blood:	n/a
3	chr4:99235909-99235959	MCF-7	breast:	n/a
4	chr4:99182798-99182848	GM12891	blood:	n/a
5	chr4:99182798-99182848	NHDF-neo	bronchial:	n/a
6	chr4:99389164-99389214	HCF	heart:	n/a
7	chr4:99186446-99186496	HCF	heart:	n/a
8	chr4:99183198-99183248	HRE	kidney:	n/a
9	chr4:99182242-99182292	ProgFib	skin:	n/a
10	chr4:99388993-99389043	HRPEpiC	eye:	n/a
11	chr4:99159401-99159451	HCT-116	colon:	n/a
12	chr4:99388850-99388900	AoSMC	blood vessel:	n/a
13	chr4:99125084-99125134	ECC-1	luminal epithelium:	n/a
14	chr4:99178293-99178343	HEK293	kidney:	embryo
15	chr4:99388941-99388991	HL-60	blood:	n/a
16	chr4:99407996-99408046	HCF	heart:	n/a
17	chr4:99388993-99389043	BJ	skin:	n/a
18	chr4:99393613-99393663	SK-N-SH	brain:	n/a
19	chr4:99159401-99159451	SAEC	small airway:	n/a
20	chr4:99182798-99182848	MCF-7	breast:	n/a
21	chr4:99182798-99182848	RPTEC	kidney:	n/a
22	chr4:99389164-99389214	Jurkat	blood:	n/a
23	chr4:99182798-99182848	K562	blood:	n/a
24	chr4:99182242-99182292	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:99159401-99159451	MCF10A-Er-Src	breast:	n/a
26	chr4:99125084-99125134	K562	blood:	n/a
27	chr4:99407996-99408046	MCF10A-Er-Src	breast:	n/a
28	chr4:99182798-99182848	BJ	skin:	n/a
29	chr4:99410748-99410798	SK-N-SH	brain:	n/a
30	chr4:99410748-99410798	SKMC	muscle:	n/a
31	chr4:99404186-99404236	HRPEpiC	eye:	n/a
32	chr4:99182242-99182292	HEK293	kidney:	embryo
33	chr4:99182798-99182848	SK-N-MC	brain:	n/a
34	chr4:99182328-99182378	HIPEpiC	eye:	n/a
35	chr4:99182555-99182605	H1-hESC	embryonic stem cell:	embryo
36	chr4:99388941-99388991	IMR90	lung:	fetal
37	chr4:99182555-99182605	HCT-116	colon:	n/a
38	chr4:99410748-99410798	HEEpiC	esophagus:	n/a
39	chr4:99388850-99388900	ovcar-3	ovarian:	n/a
40	chr4:99182242-99182292	CMK	blood:	n/a
41	chr4:99183198-99183248	HAEpiC	amniotic membrane:	n/a
42	chr4:99363399-99363449	AG04450	lung:	fetal
43	chr4:99388993-99389043	AG09309	skin:	n/a
44	chr4:99389164-99389214	HEEpiC	esophagus:	n/a
45	chr4:99393613-99393663	HAEpiC	amniotic membrane:	n/a
46	chr4:99402843-99402893	ECC-1	luminal epithelium:	n/a
47	chr4:99410748-99410798	ECC-1	luminal epithelium:	n/a
48	chr4:99388941-99388991	PFSK-1	brain:	n/a
49	chr4:99410748-99410798	NHDF-neo	bronchial:	n/a
50	chr4:99182328-99182378	HRCEpiC	kidney:	n/a

(count:143 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:99171483..99174097-chr4:99174454..99176664,2	MCF-7	breast:
2	chr4:99281508..99283161-chr4:99283275..99285281,2	MCF-7	breast:
3	chr4:99064189..99066561-chr4:99135372..99138314,2	MCF-7	breast:
4	chr4:99034025..99034574-chr4:99308766..99309435,2	MCF-7	breast:
5	chr4:99180881..99186469-chr4:99190114..99194249,6	K562	blood:
6	chr4:99232667..99234640-chr4:99237819..99239582,2	MCF-7	breast:
7	chr4:99402389..99404917-chr4:99406688..99409637,2	K562	blood:
8	chr4:99071301..99072792-chr4:99120456..99121365,4	MCF-7	breast:
9	chr4:99177008..99180462-chr4:99180782..99182422,3	K562	blood:
10	chr4:99275967..99278329-chr4:99281656..99283671,2	K562	blood:
11	chr4:99169147..99171084-chr4:99176723..99180239,3	K562	blood:
12	chr4:99205046..99207834-chr4:99212781..99214313,2	MCF-7	breast:
13	chr4:99319259..99322720-chr4:99325814..99328439,4	K562	blood:
14	chr4:99235218..99237306-chr4:99238634..99241248,2	MCF-7	breast:
15	chr4:99314967..99316909-chr4:99316924..99318922,2	K562	blood:
16	chr4:99319259..99322720-chr4:99325814..99328439,4	K562	blood:
17	chr4:99409324..99410848-chr4:99410928..99413452,2	MCF-7	breast:
18	chr4:99181854..99184121-chr4:99363566..99365529,2	MCF-7	breast:
19	chr4:99182748..99183661-chr6:89791487..89792153,2	Hela-S3	cervix:
20	chr4:99072160..99072897-chr4:99308436..99309402,2	MCF-7	breast:
21	chr4:99317366..99319383-chr4:99320195..99322035,2	K562	blood:
22	chr4:99314982..99316976-chr4:99318603..99320345,2	K562	blood:
23	chr4:99071303..99072113-chr4:99388789..99389313,2	MCF-7	breast:
24	chr4:99314967..99316909-chr4:99316924..99318922,2	K562	blood:
25	chr4:99183041..99184683-chr4:99227227..99228735,2	MCF-7	breast:
26	chr4:99297214..99300431-chr4:99303291..99306046,3	K562	blood:
27	chr4:99181700..99182466-chr6:132272011..132272954,2	HCT-116	colon:
28	chr4:99275967..99278329-chr4:99281656..99283671,2	K562	blood:
29	chr4:99063959..99066263-chr4:99181971..99183968,2	K562	blood:
30	chr4:99187002..99188810-chr4:99194814..99197047,2	K562	blood:
31	chr4:99298931..99300535-chr4:99303915..99306046,2	K562	blood:
32	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
33	chr4:99284843..99287176-chr4:99294618..99297593,2	K562	blood:
34	chr4:99063973..99066325-chr4:99305567..99308333,2	MCF-7	breast:
35	chr4:99309632..99312263-chr4:99316349..99318716,2	K562	blood:
36	chr4:99185202..99187066-chr4:99307470..99310118,2	K562	blood:
37	chr4:99320884..99324125-chr4:99325864..99328439,3	K562	blood:
38	chr14:20923127..20923687-chr4:99285884..99286471,2	HCT-116	colon:
39	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
40	chr4:99168522..99170647-chr4:99175545..99178223,2	K562	blood:
41	chr4:99184237..99185798-chr4:99187404..99189518,2	K562	blood:
42	chr4:99300207..99302055-chr4:99309249..99311340,2	MCF-7	breast:
43	chr4:99235218..99237306-chr4:99238634..99241248,2	MCF-7	breast:
44	chr4:99368820..99371256-chr4:99372389..99374542,2	K562	blood:
45	chr4:99368820..99371256-chr4:99372389..99374542,2	K562	blood:
46	chr4:99184237..99185798-chr4:99187404..99189518,2	K562	blood:
47	chr4:99187002..99188810-chr4:99194814..99197047,2	K562	blood:
48	chr4:99388436..99389361-chr4:99666672..99667178,2	MCF-7	breast:
49	chr4:99180371..99183647-chr4:99401160..99403823,3	MCF-7	breast:
50	chr4:99181367..99183940-chr4:99249153..99251764,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf37-2	chr4:99182703-99182781	ENSG00000214559.3
2	lnc-C4orf37-2	chr4:99172839-99173156	ENSG00000214559.3
3	lnc-C4orf37-1	chr4:99104226-99104923	XLOC_004020
4	lnc-C4orf37-1	chr4:99106282-99106355	XLOC_004020
5	lnc-METAP1-7	chr4:99330441-99330914	NONHSAT097488

No data

Variant related genes	Relation type
ENSG00000251523	TF binding region
ENSG00000200658	TF binding region
TSPAN5	TF binding region
ENSG00000242318	TF binding region
RAP1GDS1	TF binding region
ENSG00000214559	TF binding region
ENSG00000251523	CpG island
ENSG00000200658	CpG island
TSPAN5	CpG island
ENSG00000242318	CpG island
RAP1GDS1	CpG island
ENSG00000214559	CpG island
ENSG00000112715	chromatin interactions
ENSG00000163116	chromatin interactions
ENSG00000101146	chromatin interactions
ENSG00000260641	chromatin interactions
ENSG00000227220	chromatin interactions
ENSG00000168785	chromatin interactions
ENSG00000184277	chromatin interactions
ENSG00000138698	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000200658	chromatin interactions
ENSG00000100823	chromatin interactions
ENSG00000118523	chromatin interactions
ENSG00000103064	chromatin interactions
ENSG00000146278	chromatin interactions
ENSG00000042753	chromatin interactions
ENSG00000092094	chromatin interactions

Extended variants
information (count: 10135 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:10135 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13150465	chr4:99094892-99094893	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569805792	chr4:99094917-99094918	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375507847	chr4:99094989-99094990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186542181	chr4:99095002-99095003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113943929	chr4:99095060-99095061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4699606	chr4:99095074-99095075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4699607	chr4:99095084-99095085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs139582753	chr4:99095205-99095206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545813888	chr4:99095236-99095237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191299334	chr4:99095239-99095240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112657029	chr4:99095240-99095241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142597302	chr4:99095245-99095246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4699608	chr4:99095281-99095282	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs562281296	chr4:99095302-99095303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559825439	chr4:99095322-99095323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144015685	chr4:99095409-99095410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183602515	chr4:99095430-99095431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369869234	chr4:99095488-99095489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10032272	chr4:99095601-99095602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188239698	chr4:99095677-99095678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551346235	chr4:99095689-99095690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542972029	chr4:99095725-99095726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569740459	chr4:99095803-99095804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148702748	chr4:99095807-99095808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544083206	chr4:99095849-99095850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555593068	chr4:99095855-99095856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568204470	chr4:99095912-99095913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535295926	chr4:99095915-99095916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113730400	chr4:99095935-99095936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190512305	chr4:99095938-99095939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565906288	chr4:99095940-99095941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151211515	chr4:99095963-99095964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557765126	chr4:99096023-99096024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576129852	chr4:99096082-99096083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543471969	chr4:99096101-99096102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561639199	chr4:99096169-99096170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139460999	chr4:99096187-99096188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541256041	chr4:99096219-99096220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113215317	chr4:99096227-99096228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377030649	chr4:99096240-99096241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75894715	chr4:99096271-99096272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533424552	chr4:99096289-99096290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551675773	chr4:99096292-99096293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563305550	chr4:99096298-99096299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551605426	chr4:99096309-99096310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183092673	chr4:99096350-99096351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7656196	chr4:99096380-99096381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567652665	chr4:99096413-99096414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369179476	chr4:99096418-99096419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537234295	chr4:99096426-99096427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Oral squamous cell carcinoma	17134496	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:4861 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99088200-99098200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:99092200-99097000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:99092400-99097400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:99092600-99097200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:99092600-99097200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:99092600-99097200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr4:99092600-99097600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:99092800-99097000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:99093000-99098200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:99097000-99097600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:99097000-99098200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:99097000-99099000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:99097200-99098000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:99097200-99098400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:99097200-99098400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:99097400-99097800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:99097600-99098200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr4:99097600-99098800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:99097600-99099600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:99097800-99098200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr4:99098000-99100800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr4:99098200-99098600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:99098200-99098600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:99098200-99098600	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr4:99098400-99099200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:99098400-99101400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr4:99098600-99099200	Enhancers	Fetal Brain Male	brain
28	chr4:99098600-99099200	Enhancers	Fetal Brain Female	brain
29	chr4:99098600-99100400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:99099200-99100000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:99099200-99100200	Weak transcription	Fetal Brain Male	brain
32	chr4:99099200-99100400	Weak transcription	Fetal Brain Female	brain
33	chr4:99099600-99100400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:99099600-99102000	Enhancers	Fetal Lung	lung
35	chr4:99100000-99101400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:99100200-99101600	Enhancers	Fetal Brain Male	brain
37	chr4:99100400-99100600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:99100400-99100600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:99100400-99100600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:99100400-99101000	Enhancers	Fetal Brain Female	brain
41	chr4:99100600-99101600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:99100600-99101600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr4:99100800-99101000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:99101000-99101400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:99101000-99101600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:99101400-99101600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:99101400-99101600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:99101600-99104800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:99101800-99108800	Weak transcription	Primary B cells from cord blood	blood
50	chr4:99104800-99105400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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